Process for making esters of 2-acetoxyalkanoic acids using a 3,6-dialkyl-1,4-dioxane-2,5-dione or poly-(alpha-hydroxyalkanoic acid) as a starting material
View Patent ↗2-Acetoxyalkanoic acid esters are made in a reaction of a 3,6-dialkyl-1,4-dioxane-2,5-dione or a poly(α-hydroxyalkanoic acid), an acetate ester and an alcohol or phenol in the presence of a transesterification catalyst. Unlike previous methods for making 2-acetoxyalkanoic acid esters, this process proceeds in high yield and high selectivity to the desired product.
1. A process for making a 2-acetoxyalkanoic acid ester comprising heating a mixture of a poly(α-hydroxyalkanoic acid) having a number average degree of polymerization of at least 8 and a combined concentration of water and carboxyl groups of no greater than 2 moles/kg with an acetate ester having the structure
wherein the acetate ester is provided in excess in relation to the moles of α-hydroxyalkanoic acid repeating units in the starting poly(α-hydroxyalkanoic acid), to a temperature of at least 150° C. under superatmospheric pressure in the presence of a transesterification catalyst to convert at least a portion of the poly(α-hydroxyalkanoic acid) to a 2-acetoxyalkanoic acid ester having the structure
wherein R is an unsubstituted or inertly substituted alkyl group and R 1 is linear, branched or cyclic alkyl or aryl, and wherein the transesterification catalyst is selected from the group consisting of an alkyl or aryl sulfonic acid compound, hydrochloric acid, sulfuric acid, phosphoric acid, an oligomer of phosphoric acid, tin chloride, tin oxide, a dialkyl tin oxide, an alkyltinalkoxide, an alkyltincarboxylate, and boron trifluoride.
2. The process of claim 1 which is performed in the presence of at least 0.8 moles of an alkanol or phenol having the structure R 1 —OH, wherein R 1 is a linear, branched or cyclic alkyl or phenyl per mole of α-hydroxyalkanoic acid repeat unit in the poly(α-hydroxyalkanoic acid).
3. The process of claim 2 , wherein the acetate ester is methyl acetate and the alkanol is methanol.
4. The process of claim 2 , wherein the acetate ester is phenyl acetate and the alkanol or phenol is phenol.
5. The process of claim 2 , wherein the acetate ester is n-butyl acetate and the alkanol is n-butanol.
6. The process of claim 1 , further comprising recovering the 2-acetoxyalkanoic acid ester.
7. The process of claim 6 , wherein the 2-acetoxyalkanoic acid ester is recovered by crystallization or distillation.
8. The process of claim 1 , wherein the conversion of the starting poly(α-hydroxyalkanoic acid) having a number average degree of polymerization of at least 8 is at least 90%.
9. The process of claim 1 wherein the transesterification catalyst is selected from the group consisting of para-toluene sulfonic acid and tin chloride.