PROCESS FOR PRODUCING (R)-3-HYDROXYBUTYL (R)-3-HYDROXYBUTYRATE

Abstract

Embodiments of the present invention are directed to processes for the production of (R)-3-hydroxybutyl (R)-3-hydroxybyrate. Poly (R)-3-hydroxybyrate is transesterified with an alcohol, to form a first ester portion and a second ester portion. The first ester portion is reduced to the diol to form a diol portion and the diol portion is reacted with the second ester portion to produce (R)-3-hydroxybutyl (R)-3-hydroxybyrate.

Claims

1. A process for the production of (R)-3-hydroxybutyl (R)-3-hydroxybutyrate comprising: (i) contacting poly-(R)-3-hydroxybutyrate with an alcohol to transesterify the poly-(R)-3-hydroxybutyrate under transesterification conditions to produce an ester of (R)-3-hydroxybutyrate and the alcohol; (ii) separating the product of step i) into a first and second portion and reducing the first portion of the (R) 3-hydroxybutyrate ester to form (R)-1,3-butanediol; (iii) contacting under transesterification conditions the (R)-1,3-butanediol from step ii) with the second portion of the transesterified ester to produce (R)-3-hydroxybutyl-(R)-hydroxybutanoate.

2. A process according to claim 1 wherein the poly-(R)-3-hydroxybutyrate is obtained from corn starch or sugar cane.

3. A process according to claim 1 wherein the poly-(R)-3-hydroxybutyrate is transesterified in step i) using ethanol.

4. A process according to claim 1 wherein the weight ratio of alcohol to poly-(R)-3-hydroxybutyrate is from 1:1 to 10:1.

5. A process according to claim 1 wherein the step i) is carried out in acidic conditions.

6. A process according to claim 1 wherein the product of step i) is treated to neutralise the acid, remove the alcohol by distillation.

7. A process according to claim 6 wherein the distillation is carried out at a temperature of 110° C. to 150° C.

8. A process according to claim 1 wherein the reduction in step ii) comprises reducing (R)-3-hydroxybutyrate ester using a hydride transfer reagent.

9. A process according to claim 8 wherein the reducing agent is selected from lithium aluminium hydride, sodium bis (2-methoxyethoxy) aluminium hydride, sodium borohydride, nickel borohydride.

Description

Example 1

[0034] Transesterification Step i)

[0035] A 5 gallon Parr reactor is charged with 12.5 L(10 kg) absolute ethanol and 2.5 kg poly (R)-3-hydroxybutanoate (Biocycle, Fazenda de Pedra, c Postal 02 CEP 14158-00, Serenaa, S. P. Brazil) and stirred for 2-5min to complete mixing after which 0.1 L concentrated sulfuric acid is added slowly to the mixture, The mixture is heated with a 300° C./h ramp to 110° C. and the reactor held in soak mode for a total run time is 22 h. The unit is cooled to about 30° C. using chilled water. After the temperature has fallen below 60° C., the digester is vented and purged with nitrogen to remove formed ether. An amount of base, equal to the equivalents of acid is added to the crude digest with stirring to neutralize the acid. Stirring is continued about 16 h after which the stirring is stopped and the solids left to settle. The liquid phase is siphoned off into a wiped film distillation apparatus and distilled in phases to remove first the ethanol and ethyl crotonate (a side product), and then the ethyl (R)-3-hydroxybutyrate. Ethanol/ethyl crotonate is distilled off over 3 passes generally at atmospheric pressure and band heater and pump flow rates of 120 & 5 L/h, 120 & 3 L/h and 140 & 3 L/h respectively. The ethyl (R) 3-hydroxybutyrate is distilled at 10 mmHg, band heater=88 and feed rate 4 L/h. The primary chiller is set to 5° C. and the secondary chiller at −1° C. for all distillations. The trap is charged with dry ice and either acetone or IPA. When collecting the ethyl (R) 3-hydroxybutyrate, the residue from the first pass is recycled through the still to recover more product. The ethyl-(R)-3-hydroxybutyrate is assayed by GC-MS and NMR for purity.

[0036] Reduction Step ii)

[0037] A heavy duty stainless steel stock pot is charged with 12 L water and a portion of (3.49 L) ethyl (R) 3-hydroxybutyrate. Both water and ester were previously chilled to 4° C. for at least 24 h. The stock pot is surrounded by ice, gassed with nitrogen and stirred. After about 1 h, 1 Kg sodium borohydride is added in small aliquots to order to minimize temperature gain. Borohydride addition takes about 1 h and the temperature should be kept below 20° C. during the NaBH.sub.4 addition. About 5 h after borohydride addition the reaction is quenched by slowly adding 745 ml concentrated sulfuric acid. The mixture is allowed to stand, with stirring overnight and the temperature rise to room temperature. The mixture is filtered, the filtrate heated to 90° C. and neutralized* by adding calcium hydroxide with stirring. After 2 hours mixture is cooled and filtered and the filtrate ionic strength reduced using ion exchange resins after which the solution is placed on a Buchi Rotovap and the bulk of the water removed. This leaves a viscous liquid assaying to >10 M (R) 1,3-butanediol and containing 5-10% water. Remaining water is removed by nitrogen purge or distillation. The purity is checked by enzymatic assay, GC-MS and NMR.

[0038] Transesterification Using R-1,3-butanediol

[0039] A solution is prepared by combining and mixing 600 ml of (R) 1,3-butanediol and 1200 ml of ethyl (R)-3-hydroxybutanoate in a stainless steel pan. A nylon mesh “tea bag” containing lipase is laid in the solution and the pan is placed on a heating pad set to 40° C. The “tea bag” is sewn with lanes to keep the enzyme dispersed. The reaction is carried out under nitrogen with agitation. After 6 h the reaction is stopped by removing the “tea bag” and collecting the solution. The solution is passed through a filter to remove any enzyme resin “fines” and collected. Once enough crude solution has been collected the solution is distilled sequentially to first degas and remove any remaining ethanol, then to remove ethyl (R)-3-hydroxybutanoate, (R) 1,3-butanediol and finally to collect the desired pure ketone ester, (R)-3-hydroxybutyl (R)-3-hydroxybutyrate. Recovered ethyl (R)-3-hydroxybutanoate and (I) 1,3-butanediol are recycled in subsequent transesterification experiments. Crude solutions and still fractions are analyzed by GC-MS.