Method for preparing polyesters having intrachain free acid functions
View Patent ↗The invention relates to a method for preparing polyesters A containing several mid-chain free acid functions by ring-opening polymerisation in the presence of a chain initiator: the benzyl diester of the tartaric acid, the phenyl radical of which is optionally substituted. A: aliphatic based on cyclic esters such as lactides and glycolides.
1. A process for the preparation of a polyester containing several free acid functions arranged in the middle of the chain, based on a member of the group consisting of L-lactic acid, D-lactic acid, DL-lactic acid, ε-caprolactone, p-dioxanone, ε-caproic acid, alkylene oxalate, cycloalkylene oxalate, alkylene succinate, β-hydroxybutyrate, substituted or non-substituted trimethylene carbonate, 1,5-dioxepan-2-one, 1,4-dioxepan-2-one, glycolide, glycolic acid, L-lactide, D-lactide, DL-lactide, meso-lactide; and all optically active isomers, racemates or copolymers of the latter comprising ring-opening polymerization in the presence of as a chain initiator: tartaric acid benzyl diester, the phenyl portion of the benzyl which is optionally substituted.
2. The process of claim 1 , wherein the polyester is based on a member of the group consisting of: L-lactic acid, D-lactic acid, DL-lactic acid, ε-captrolactone, p-dioxanone, ε-caprioc acid, substituted or non-substituted trimethylene carbonate, glycolide, glycolic acid, L-lactide, D-lactide, DL-lactide, meso-lactide, and all optically active isomers, racemates or copolymers of the latter.
3. The process of claim 2 , wherein the polyester is based on a member of the group consisting of: L-lactic acid, D-lactic acid, DL-lactic acid, glycolide, glycolic acid, L-lactide, D-lactide, meso-lactide; and all optically active isomers, racemates or copolymers of the latter.
4. The process of claim 1 wherein the chain initiator is unsubstituted tartaric acid benzyl diester.
5. The process of claim 1 wherein:
the preparation of a polyester by ring-opening polymerization in the presence of the chain initiator; is followed by the deprotection of the carboxy functions of the chain initiator.