Title of Invention	"A PROCESS FOR PRODUCING POLYCONDENSABLE MACROMONOMER"
Abstract	The present invention deals with the preparation of polycondensable macromonomers with high moiety of bifunctional groups in presence of a non-reactive solvent by conventional methods.The organic compound formed consist of organic compound with more than one hydroxyl group.

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This invention relates to a process for producing macromonomers, More particularly it relates to a process for preparation of macromonomers with more than one polycodensable functional groups with equal reactivity, having formula (I) in drawing accompanying this specification, wherein, R=an alkyl group with 1-40 carbon atoms R1 = hydrogen or methyl R2 = alkylene units X = bifunctional moiety F = functional group n = 3-45 Compound I is produced by direct esterification reaction of a carboxyiic group containing polymer of formula (n) in the drawing accompanying this specification and an organic compound with more than one hydroxyl group. Macromonomers are defined as reactive oligomers. They are linear and carry some functional groups, preferably at the chain ends. They are classified into addition polymerizable and condensation polymerizable macromonomers based on the nature of the terminal functional groups. The molecular weight of macromonomer ranges from 500-50.000 and particularly in the range between 1000 and 25000. The synthesis of macromonomers is described in detail in the literature.[Sivaram,S., J.Scientific and Ind.Res.,56, 1, (1997) ; Gnanou,Y., IndJ.Technol., 31,317, (1993); Corner,!., Adv.Polym.Sci., 62 , 95, (1984); Rerapp.P.E, Adv.Polym.Sci., 58 ,53, (1981)] Macromonomers are generally produced by ionic living polymerization, group transfer polymerization and free radical polymerisation techniques. Of these, the radical routes of producing macroraonotner are commercially well acceptable, as it does not require rigorous experimental conditions. Also, the number of monomers amenable to free radical polymerization is large. Macromonomers are useful in the production of tailor made graft copolyraers and find application as surface active agents, compatibilizers, adhesion promoter, organic coatings, and biomaterials. Preparation of macromonomers via free radical method and/or by condensation method is known in the prior art In one such application, U.S.Patent 5066759 describes a process for preparing macromonomer with two antagonists functional groups. Herein the macromonomer is produced by the reaction between a diisocyanate and a prepolymer with carboxyl group at one end and hydroxyl or amino group at the other end. According to this disclosure the macromonomer contains carboxyl group at one end and hydroxyl or amino group at the other end. However the diisocyanate may also react with the carboxyl group and would not yield a macromonomer with a well-defined terminal functionality. Eur.Pat.Appl. 248574 (ChemAbst. 108:187481 w) describes the preparation of carboxy group containing hydrophilic macromonomer. Herein, the functional group is derived from initiator fragments. U.S.PaL 5254632 describes a process for producing macromonomer through a transesterification reaction between hydroxyl terminated polyalkylmethacrylate and monomeric ester. U.S Patent 5185421 describes the preparation of fluorinaied macromonomer with one or more hydroxyl group. U.S.Patent 4818804 describes the preparation of macromonotners derived from vinyl monomers and mercapto compounds. The polycondensable macromonomer thus obtained contains one or more carboxyl groups, which are attached to primary and secondary carbon atoms. This induces a difference in reactivity of the functional groups and limits the usage of such macromonomer in isocyanate polyaddition or polyesteriiication reactions. In prior art, the polycondensable macromonomers with antagonist functional groups are obtained by step growth polymerization that contains ill-defined terminal functional groups. Macromonomers produced through radical transfer reaction contains one or more terminal functional groups with different reactivity and limits its usage in further polymerization reactions. Prior at given is not sufficient and the drawbacks vis a vis the need of the alleged invention needs to be given in detail The object of the present invention is to provide a method for the preparation of polycondensable macromonomer by free radical polymerization. Another objective of the present invention is that the polycondensable groups in the macromonomer possess equal reactivity. Accordingly, the present invention provides a process for the preparation of macromonomers by reacting a carboxyl or hydroxyl terminated prepolymers, with an organic compound, containing two or more isocyanate reactive functional groups, in presence of a dehydrating agent and a non-reactive solvent at ambient temperature for a period ranging between 3 and 12 hours, separating the product from the reaction mixture by conventional methods. In an embodiment of the present invention the carboxyl or hydroxyi group containing prepolymer is prepared by polymerizing a monomer of the formula (HI), in the drawing accompanying this specification which are exemplified by methyl methacrylate. butyl methacrylate, lauryl memacrylate, ethyl acrylate, butyl acrylate, hexyl acrylate, n-octyl acrylate, 2-ethylhexyl acrylate, nonyl acrylate, lauryl acrylate and styryl acrylate in presence of a bifunctional agent of the formula (IV) or (V) in the drawing accompanying this specification which includes but not limited to mercaptoacetic acid, 3-mercaptopropionic acid, mercaptosuccinic acid, 2-mercapto ethanol, l-mercapto-2-propanol and 3-mercapto-l-propanol. In another embodiment of the present invention the multifunctional organic compounds are reactive in the context of esterification reaction which are exemplified by trimetiiylol propane, ditrimethylol propane, 1,2,6-hexane triol (its isomers), pentaerythrytol, di and tripentaerythrytol, sorbitol and glycerine. In still anodier embodiment of die present invention die dehydrating agent used includes, but not limited to, dicyclohexylcarbodiimide, N,N'carbonyldiimidazole, dicyclohexylcarbodiimide and aminopyridine, phenyl dichlorophosphate, chlorosulfonyl isocyanate, chlorosilanes, alkyl chlorofonnate - trietiiyl amine, pyridinium salts-tributyl amine, 2-chloro-l,3.5-u-initrobetizene -pyridine and phosphate ester. In yet another embodiment of the present invention the solvents used are non reactive towards the prepolymer, multifunctional organic compounds and the dehydrating agent which are exemplified by chlorinated hydrocarbons, esters, ethers, ketoesters, aliphatic, aromatic and alicyclic hydrocarbons, hydrogenated lurans and the mixtures thereof. In a feature of the present invention, the polymerization can be carried out in any conventional resin reactor equipped with a cooling jacket, a double walled condenser, a therraowell, and an addition funnel for monomer feeding. Stirring can be done by using a magnetic stirrer or by any stirring device. The polymerization reaction can be carried out between 40°C and 100°C and more preferably between 60°C and 90°C. The reaction is exothermic in the beginning and can be controlled by circulating cool water or by drop wise feeding of monomer. The desired molecular weight of the macromonomer is obtained by,adjusting molar ratio of bifunctional agent to monomer. The amount in mol percentage of die bifunctional agent based on the amount of monomer charged is preferably in the range between 1 and 45. The polymerization is initiated by the addition of initiator which have a decomposition half life at 70±10CC is £ 8 hours, which are exemplified by 2,2'-azobis-2-methyl butyronitrile, 2,2'-azobis-isobutyronitrile, 2,2'-azobis-2-cyclopentyl propionitrile and di-(2-hydroxypropyl) -2,2'-azobis-isobutyrate. The polymerization begins rapidly when the decomposition temperature of the initiator is reached. The reaction is continued until the disappearance of double bond as evident from the !H NMR spectrum. The polymer obtained is recovered by precipitation in methanol. In yet another feature of the present invention, the macromonomer with polycondensable functional group is obtained by the esterification reaction between the prepolytner and an organic compound with two or more functional groups. The esterification reaction is carried at ambient temperature in the presence of carboxyl group activator (CGA) or hydroxyl group activator (HGA). Advantageously by adopting these esterification procedure one can react a carboxy functional or hydroxy functional containing prepolymer with an organic compound having two or more hydroxyl or carboxyl group respectively, at ambient temperature. The reaction is carried out by mixing the prepolymer in a suitable solvent The prepolymer solution is preferably cooled between 0°C to 15°C and then the multifunctional organic compound and the dehydrating agent are added Alternatively, the prepolymer solution can also be added to a cooled mixture of multifunctional organic compound and the dehydrating agent The ambient temperature esterification reactions disclosed in the present invention are very fast and are completed within 1 to 6 hours. The urea formed during the reaction if filtered off and the product is recovered by distilling the solvent The process for the present invention is described herein below with examples which are illustrative only and should not be construed to limit the scope of the present invention in any manner. Example 1-6: These examples illustrate the preparation of polycondensable macromonomer from a carboxyl containing prepolymer, an organic multifunctional group and a dehydrating agent Example 1: In a three neck 100 ml round bottom flask fitted with a thermowell, condenser, a magnetic needle and a glass tube for nitrogen purging, charged 25 grain laurylmethacrylate, 3.6 gram mercapto acetic acid, 0.16 gram azobis isobutyronitrile and 29 mL toluene. The reaction mixture is stirred by means of a magnetic stirrer and nitrogen gas is purged continuously. The flask is then heated up to 80° C. The reaction is continued till the disappearance of olifmic signals in JH NMR spectrum. The polymer obtained is precipitated in methanol, washed thoroughly with methanol. The solvent is allowed to evaporate and the polymer is dried under vacuum at room temperature. In a separate three neck 100 mL round bottom flask fitted with a condenser, a magnetic needle and a glass tube for nitrogen purging, 3 gram of die above prepolymer is taken and added 50 mL dry dichloromethane. The temperature of the flask is maintained between 0°C and 5°C. 0.9 gram dicyclohexyl carbodiimide, 25 milligram dimethyl aminopyridine are then added followed by 0.8 gram trimethylol propane. The reaction is continued for 3 to 6 hours. Urea formed during the reaction is removed and the product is obtained by evaporating the filtrate. Example 2 : In a three neck 100 mL round bottom flask fitted with a thermowell, condenser, a magnetic needle and a glass tube for nitrogen purging, charged 25 gram laurylmethacrylate, 1.8 gram mercapto acetic acid, 0.16 gram azobis isobutyronitrile and 29 mL toluene. The reaction mixture is stirred by means of a magnetic stirrer and nitrogen gas is purged continuously. The flask is then heated up to 80° C. The reaction ia continued till the disappearance of oiifmic signals in 1H NMR spectrum The polymer obtained is precipitated in methanol, washed thoroughly with methanol. The solvent is men allowed to evaporate and the polymer is dried under vacuum at room temperature. In a separate three neck 100 ml round bottom flask fitted widi a condenser, a magnetic needle and a glass tube for nitrogen purging, 3grain of the above prepolymer is taken and added 50 mL dry dichloromethane. The temperature of die flask is maintained between 0°C and 5°C. 0.5 gram dicyclohexyl carbodiimide, 25 milligram dimethyl aminopyridine are men added followed by 0.43 gram trimethylol propane. The reaction is continued for 3 to 6 hours. Urea formed during die reaction is removed and me product is obtained by evaporating the filtrate. Example 3: In a diree neck 100 mL round bottom flask fitted widi a diennowell, condenser, a magnetic needle and a glass tube for nitrogen purging, charged 25 gram laurylmethacrylate, 0.73 gram mercapio acetic acid, 0.16 gram azobis isobutyronitrile and 29 mL toluene. The reaction mixture ia stirred by means of a magnetic stirrer and nitrogen gaa is purged continuously. The flask is men heated up to 80° C. The reaction is continued till die disappearance of oiifmic signals in 1H NMR spectrum. The polymer obtained is precipitated in methanol, washed ttioroughly wim memanol. The solvent is dien allowed to evaporate and die polymer is dried under vacuum at room temperature. In a three neck 100 mL round bottom flask fitted with a condenser, a magnetic needle and a glass tube for nitrogen purging, 3 gram of the above prepolymer is taken and added 50 mL dry dichloromethane. The temperature of the flask is maintained between 0°C and 5°C. 0.2 gram dicyclohexyl carbodiimide, 25 milligram dimethyl aminopyridine are men added followed by 0.16 gram trimethylol propane. The reaction is continued for 3 to 6 hours. Urea formed during the reaction is removed and die product is obtained by evaporating the filtrate. Example 4 : In a three neck 100 mL round bottom flask fitted with a thermowell, condenser, a magnetic needle and a glass tube for nitrogen purging, charged 25 gram methyl methacrylate, 3.6 gram mercapto acetic acid, 0.16 gram azobis isobutyronitrile and 29 mL toluene. The reaction mixture is stirred by means of a magnetic stirrer and nitrogen gas is purged continuously. The flask is then heated up to 80° C. The reaction is continued till the disappearance of olifinic signals in !H NMR spectrum. The polymer obtained is precipitated in methanol, washed thoroughly with methanol. The solvent is then allowed to evaporate and the polymer is dried under vacuum at room temperature. In a mree neck 100 mL round bottom flask fitted with a condenser, a magnetic needle and a glass tube for nitrogen purging, 3 gram of the above prepolymer is taken and added 50 mL dry dichloromemane. The temperature of the flask is maintained between 0°C and 5°C. 0.93 gram dicyclohexyl carbodiimide, 25 milligram dimethyl aminopyridine are then added followed by 0.8 gram trimethylol propane. The reaction is continued for 3 to 6 hours. Urea formed during the reaction is removed and the product is obtained by evaporating the filtrate. Example 5 ; In a three neck 100 mL round bottom flask fitted with a thermowell, condenser., a magnetic needle and a glass tube for nitrogen purging, charged 25 gram methyl methacrylate, 1.8 gram mere apt o acetic acid, 0.16 gram azobis isobutyronitrile and 29 mL toluene. The reaction mixture is stirred by means of a magnetic stirrer and nitrogen gas is purged continuously. The flask is then heated up to 80C C. The reaction is continued till the disappearance of olifmic signals in 1H NMR spectrum. The polymer obtained is precipitated in methanol, washed thoroughly with methanol. The solvent is then allowed to evaporate and me polymer is dried under vacuum at room temperature. In a three neck 100 mL round bottom flask fitted with a condenser, a magnetic needle and a glass tube for nitrogen purging, 3 gram of the above prepolymer is taken and added 50 mL dry dichloromethane. The temperature of the flask is maintained between 0°C and 5°C. 0.5 gram dicyclohexyl carbodiimide, 25 milligram dimethyl aminopyridine are then added followed by 0.43 gram trimethylol propane. The reaction is continued for 3 to 6 hours. Urea formed during the reaction is removed and the prqduct is obtained by evaporating the filtrate. Example 6 : In a three neck 100 mL round bottom flask fitted with a thennowell, condenser, a magnetic needle and a glass tube for nitrogen purging, charged 25 gram methyl methacrylate, 0.72 gram mercapto acetic acid, 0.16 gram azobis isobutyronitrile and 29 mL toluene. The reaction mixture is stirred by means of a magnetic stirrer and nitrogen gas is purged continuously. The flask is then heated up to 80° C. The reaction is continued till the disappearance of olifmic signals in 1H NMR spectrum. The polymer obtained is precipitated in methanol, washed thoroughly with methanol. The solvent is then allowed to evaporate and the polymer is dried under vacuum at room temperature. In a three neck 100 mL round bottom flask fitted with a condenser, a magnetic needle and a glass tube for nitrogen purging, 3 gram of the above prepolymer is taken and added 50 mL dry dichloromemane. The temperature of the flask is maintained between 0°C and 5CC. 0.2 gram dicyclohexyl carbodiimide, 25 milligram dimethyl aminopyridine are then added followed by 0.16 gram trimethylol propane. The reaction is continued for 3 to 6 hours. Urea formed during the reaction is removed and die product is obtained by evaporating the filtrate. Example 7: This examples illustrate the preparation of polycondensable macromonomer from a hydroxyl group containing prepolymer, an organic multifunctional group and a dehydrating agent In a diree neck 100 ml round bottom flask fitted widl a mermovvell, condenser, a magnetic needle and a glass tube for nitrogen purging, charged 25 gram laurylmemacrylate, 3.0 gram mercapto ethanol, 0.16 gram azobis isobutyronitrile and 29 mL toluene. The reaction mixture is stirred by means of a magnetic stirrer and nitrogen gas is purged continuously. The flask is then heated up to 80° C. The reaction is continued till the disappearance of olifinic signals in 'H NMR spectrum. The polymer obtained is precipitated in niethanol, washed thoroughly with methanol. The solvent is allowed to evaporate and the polymer is dried under vacuum at room temperature. In a separate three neck 100 mL round bottom flask fitted with a condenser, a magnetic needle and a glass tube for nitrogen purging, 3 gram of the above prepolymer is taken and added 50 mL dry dichloromethane. The temperature of the flask is maintained between 0°C and 5°C. 1.2 gram dicyclohexyl carbodiimide, 25 milligram dimethyl aminopyridine are then added followed by 0.8 gram dimethylol propionic acid The reaction is continued for 3 to 6 hours. Urea formed during the reaction is removed and the product is obtained by evaporating me filtrate. WE CLAIM: 1. A process for producing polycondensable macromonomers having formula (I) in the drawing accompanying the specification, wherein, R=an alkyl group with 1-40 carbon atoms R'=hydrogen or methyl R2=alkylene units X=bifunctional moiety F=functional group n-3-45 m=>2 which comprises reacting a carboxyl or hydroxyl terminated prepolymers with an organic compound containing two or more isocyanate reactive functional groups, in presence of a dehydrating agent and a non-reactive solvent at temperature ranging from 25 to 35°C for a period ranging between 3 and 12 hours, separating the product from the reaction mixture by conventional methods. 2. A process as claimed in claim 1, wherein the multifunctional organic compounds are selected from trimethylol propane, ditrimethyllol propane, 1,2,6-hexane troll(its isomers), pentaerythrytol, di and tripentaerythrytol, sorbitol and glycerine. 3. A process as claimed in claim 1, wherein the dehydrating agent used is selected from dicyclohexylcarbodiimide and amino pyridine, phenyl dichlorophosphate, chlorosulfonyl isocyanate, chlorosilanes, alkyl chloroformate-triethyl amine, pyridinium salts-tributyl amine, 2-chloro-l,3,5-trinitrobenzene-pyridine and phosphate ester. 4. A process as claimed in claim 1, wherein the solvents used are selected from chlorinated hydrocarbons, esters, ethers, ketoesters, aliphatic, aromatic and alicyclic hydrocarbons, hydrogenated furans and the mixtures thereof. 5. A process for producing polycondensable macromonomers having formula (I) substantially as herein described with reference to the examples.

Documents:

1635-DEL-1998-Abstract.pdf

1635-del-1998-claims.pdf

1635-del-1998-correspondence-others.pdf

1635-del-1998-correspondence-po.pdf

1635-del-1998-description (complete).pdf

1635-del-1998-drawings.pdf

1635-del-1998-form-1.pdf

1635-del-1998-form-19.pdf

1635-del-1998-form-2.pdf

1635-DEL-1998-Form-3.pdf

1635-del-1998-petition-138.pdf