IP Library Granted Patent US 11,566,268
Granted Patent B2
US 11,566,268 · App. 14/213,713 · Granted Jan 31, 2023

Process for producing (R)-3-hydroxybutyl (R)-3-hydroxybutyrate

Inventors: Kieran Clarke (Oxford, GB); Richard Lewis Veech (Rockville, MD); M. Todd King (Rockville, MD)
Assignees: GOVERNMENT OF THE USA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES; OXFORD UNIVERSITY INNOVATION LIMITED
C12P7/62C07C29/147C07C67/03C07B2200/07
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Quick Facts
Patent No.
US 11,566,268
App. No.
14/213,713
Granted
Jan 31, 2023
Kind
B2
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 (16)

1. A process for the production of (R)-3-hydroxybutyl-(R)-3-hydroxybutyrate from a single starting material feedstock of poly-(R)-3-hydroxybutyrate, comprising:

(i) contacting the 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, wherein the transesterification is carried out between 1 hour and 30 hours;

(ii) separating the product of step i) into a first and second portion and reducing the first portion in a solvent using a ketoreductase or an alcohol dehydrogenase to form (R)-1,3-butanediol; and

(iii) contacting under enzyme-catalyzed 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, wherein the enzyme-catalyzed transesterification is carried out between 1 hour and 20 hours.

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

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

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

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

6. The process according to claim 1 wherein the product of step (i) is treated to neutralize the acid and remove the alcohol by distillation.

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

8. The process of claim 1 , wherein prior to contacting in step (i), the process comprises fermenting a single starting material feedstock to produce the poly-(R)-3-hydroxybutyrate, wherein the feedstock is corn starch or sugar cane.

9. The process of claim 8 , wherein the feedstock is corn starch.

10. The process of claim 8 , wherein the feedstock is sugar cane.

11. The process of claim 8 , wherein the fermenting comprises using at least one microorganism.

12. The process of claim 1 , wherein the reaction mixture of step (i) comprises an acid catalyst.

13. The process of claim 1 , wherein the enzyme-catalyzed transesterification in step (iii) is carried out in the presence of lipase.

Assignments (3)
CHANGE OF NAME Recorded Aug 2, 2016
From: ISIS INNOVATION LIMITED
To: OXFORD UNIVERSITY INNOVATION LIMITED
Reel/Frame 039550/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 9, 2015
From: VEECH, RICHARD L.; KING, M. TODD
To: GOVERNMENT OF THE USA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES
Reel/Frame 036767/0874 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2015
From: CLARKE, KIERAN
To: ISIS INNOVATION LTD
Reel/Frame 036752/0776 →