Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
  • C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
  • C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
  • C07C29/147—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
  • C07C31/18—Polyhydroxylic acyclic alcohols
  • C07C31/20—Dihydroxylic alcohols
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
  • C07C31/18—Polyhydroxylic acyclic alcohols
  • C07C31/20—Dihydroxylic alcohols
  • C07C31/207—1,4-Butanediol; 1,3-Butanediol; 1,2-Butanediol; 2,3-Butanediol
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C67/00—Preparation of carboxylic acid esters
  • C07C67/02—Preparation of carboxylic acid esters by interreacting ester groups, i.e. transesterification
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C67/00—Preparation of carboxylic acid esters
  • C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
  • C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
  • C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
  • C07C69/675—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
  • C12P7/00—Preparation of oxygen-containing organic compounds
  • C12P7/62—Carboxylic acid esters
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
  • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
  • C07B2200/07—Optical isomers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
  • Y02E50/00—Technologies for the production of fuel of non-fossil origin
  • Y02E50/10—Biofuels, e.g. bio-diesel

Definitions

• the invention relates to a process for producing (R 3-hydroxybutyl (R)-3-hydroxybutyrate.
• the invention relates to a process for producing (R -3-hydroxybutyl (R)-3- hydroxybutyrate from a single starting material feedstock of poly-f/?J-3-hydroxybutyrate.
• Ketone bodies are chemical compounds which are produced by the liver from fatty acids released from adipose tissue. Ketone bodies themselves can be used as a source of energy in most tissues of the body. The intake of compounds that boost the levels of ketone bodies in the blood can lead to various clinical benefits, including an enhancement of physical and cognitive performance and the treatment of cardiovascular conditions, diabetes, neurodegenerative diseases and epilepsy. Ketone bodies include fR ⁇ -3-hydroxybutyrate and acetoacetate.
• ketone bodies may be administered directly to achieve elevated levels of ketone bodies in a subject.
• direct administration of the compounds is unpractical and potentially dangerous.
• direct administration of either f 3 ⁇ 4-3-hydroxybutyrate or acetoacetate in its free acid form can result in significant acidosis following rapid absorption from the gastrointestinal tract.
• Administration of the sodium salt of these compounds in unregulated amounts is also unsuitable due to a potentially dangerous sodium overload that could accompany administration of therapeutically relevant amounts of the compounds.
• esters for instance esters derived from a variety of alcohols and oligomers of (7?J-3-hydroxybutyrate.
• WO2010021766 discloses that one particular enantiomer of one particular ester of 3- hydroxybutyrate is an effective and palatable precursor to the ketone body (f?)-3- hydroxybutyrate.
• WO2010021766 discloses 3-hydroxybutyl 3-hydroxybutyrate enantiomerically enriched with respect to (fi)-3-hydroxybulyl ⁇ 7? 3-hydroxybutyrate.
• RECTIFIED SHEET (RULE 91 )
• WO2010/120300 discloses various methods of a producing (7?j-3-hydroxy butyl (R)-3- hydroxybutyrate involving enantioselective reduction of a compound of formula I, II or III.
• the invention provides a process for the production of (7 ⁇ -3-hydroxybutyl (7 ⁇ -3-hydroxybutyrate comprising: (i) contacting poly-fRJ-S-hydroxybutyrate with an alcohol to transesterify the poly- (RJ-S-hydroxybutyrate under transesterification conditions to produce an ester of (RJ-S-hydroxybutyrate and the alcohol;
• step i) separating the product of step i) into a first and second portion and reducing the first portion of the (RJ-S-hydroxybutyrate ester to form (R)-1 ,3-butanediol;
• enriched means that the level of the enriching isomer is higher than the level at which that isomer would be present in a racemic mixture.
• the enriching isomer constitutes that molar percentage of the total 3-hydroxybutyl 3-hydroxybutyrate product present.
• enantiomeric purity is measured using chiral high performance liquid c h omatography (chiral HPLC). Measurements are typically made against the corresponding racemic mixture.
• chiral gas c h omatography chiral GC
• the percentage enrichment is typically that measured by chiral HPLC or by chiral GC.
• the percentage enrichment is that measured by chiral HPLC.
• the enzyme employed is one which is capable of reducing said compound of formula (II), (III) or (IV) to produce 3-hydroxybutyl 3-hydroxybutyrate which is enantiomerically enriched to at least 95 %, for instance to at least 97 %, to at least 98 %, or to at least 99 %, with respect to (R)-3-hydroxybutyl(R)-3hydroxybutyrate.
• the process may be continuous or batch.
• the invention enables a high t h oughput industrial production of (RJ-S-hydroxybutyl (RJ-S-hydroxybutyrate from po ⁇ y-(R)-3- hydroxybutyrate which may be obtained from corn starch.
• the poly-fRJ-S-hydroxybutyrate feedstock is provided from a single feedstock by fermentation of corn starch with microorganisms.
• the poly-fRJ-S-hydroxybutyrate feedstock may be transesterified in step i) using any suitable alcohol which allows the formed ester to be reduced to (R)-1 ,3-butanediol.
• a dihydric or trihydric alcohol is employed but preferably the alcohol is monohydric, for example a C1 -6 alcohol.
• the alcohol is suitably ethanol as this is more acceptable for consumption than other alcohols.
• the alcohol is present in sufficient quantity that poly-fRJ-S-hydroxybutyrate moieties may be esterified.
• the weight ratio of alcohol to poly-fRJ-S-hydroxybutyrate is from 1 :1 to 10:1 , more preferably from 2:1 to 6:1 .
• the transesterification in step i) is suitably carried out in acidic conditions.
• the reaction mixture comprises an acid catalyst.
• the acid may be organic or inorganic and is preferably a mineral acid, for example sulphuric acid.
• the catalyst may be solid as desired.
• the transesterification is carried out at elevated temperature, preferably greater than 50 °C, greater than 90 °C and desirably not more than 150 °C. Elevated pressure may be employed.
• the transesterification is carried out for sufficient time to affect transesterification to an economically acceptable degree having regard to the temperature, catalyst and alcohol employed.
• the transesterification step is carried out for at least 1 hour, more preferably at least 10 hours, and especially 15 to 30 hours, for example 20 hours, 22 hours and 24 hours.
• the product of the transesterification reaction may then be treated by one or more optional steps including filtering, purification, for example by distillation and neutralisation for example by the addition of base for example hydroxide, bicarbonate and acetate, particularly calcium hydroxide or sodium bicarbonate to neutralise the acid present.
• filtering purification, for example by distillation and neutralisation for example by the addition of base for example hydroxide, bicarbonate and acetate, particularly calcium hydroxide or sodium bicarbonate to neutralise the acid present.
• the ester of (T ⁇ J-S-hydroxybutyrate is separated from the reaction mixture by removal of alcohol and optionally by-products of the reaction.
• the separation may be carried out in multiple stages as desired.
• the ester is separated and purified from the alcohol and reaction by-products.
• the ester may be separated from unreacted alcohol and other undesired materials, for example alkyl crotonate by separation of the liquid phase, for example by distillation of the alcohol and alkyl crotonate.
• the alcohol and by-products may be removed by multiple distillations, suitably at atmospheric pressure and at a temperature above the boiling point of the alcohol, for example greater than 80 °C, greater than 1 10 °C for example at a temperature of 1 10 to 150 °C.
• the ester of (R)-3- hydroxybutyrate is then suitably separated to provide a first portion which is subjected to a reduction reaction.
• the reduction in step ii) may be a hydride transfer reduction, hydrogenation, hydrosilylation followed by silyl ether hydrolysis.
• the reduction is carried out with any suitable reducing agent for reducing an ketoester.
• the reducing agent may be organic or inorganic.
• the reduction step may be mediated by an enzyme, for example a ketoreductase (KRED) or an alcohol dehydrogenase (ADH), and may be naturally occurring or commercially available, for example as described in WO2010/120300.
• KRED ketoreductase
• ADH alcohol dehydrogenase
• the reducing agent may comprise hydrogen and a hydrogenation catalyst may be employed, for example Raney nickel, desirably employed at elevated pressure and temperature and catalysts comprising platinum, palladium, rhodium, iridium or ruthenium.
• a hydrogenation catalyst for example Raney nickel, desirably employed at elevated pressure and temperature and catalysts comprising platinum, palladium, rhodium, iridium or ruthenium.
• the reducing agent employs a hydride transfer reagent.
• Suitable reducing agents include complex metal hydrides for example, lithium aluminium hydride, lithium tetrahydridoaluminate, sodium bis (2-methoxyethoxy) aluminium hydride, sodium borohydride, nickel borohydride, other inorganic reducing agents, for example, sodium hydrosulphite, sodium tetrahydroborate and ruthenium hydrogenation catalysts known in the art, for example ruthenium hydride and rhodium hydrogenation catalysts known in the art, aluminium triisopropoxide, and organic reducing agents including a chiral borane, for example 2,5-dimethylborolane, borontrihydride:tetrahydrofuran or catlcholborane, and enzymes and cofactors, for example nicotinamide adenine dinucleotide (NADH) and nicotinamide adenine dinucleotide phosphate (NADPH).
• a cofactor recycling system is suitably employed.
• the reducing step is suitably carried out under reducing conditions.
• a solvent may be employed.
• the solvent may be anhydrous, for example diethyl ether or tetrahydrofuran, or may be carried out in polar protic solvent, for example water, alcohol and basic aqueous media, depending upon the reducing agent.
• the reducing step is carried out in aqueous solution and a moderately strong reducing agent is employed so as to ensure retention of the desired stereochemistry.
• the temperature of the reducing step is controlled to avoid significant temperature rise, and is desirably carried out at a temperature below standard temperature, desirably under 10 °C, for example -5 to 3C.
• the reducing agent is contacted with the first portion slowly to avoid undue temperature rise.
• the reducing agent and first portion are suitably allowed to react over an extended period of time, for example at least 30 minute, preferably at least 1 hour, more preferably 1 to 20 hours, especially 4 to 10 hours.
• the reaction may be quenched by addition of a quenching agent, for example by addition of acid, for example sulphuric acid and allowed to stand for a period of time, for example at least 1 hour, preferably 1 to 20 hours, for example overnight. Thereafter, the reaction mixture may be contacted with a removal agent, for example hydroxide and especially calcium hydroxide to remove salts of the reducing agent and quenching agent.
• a quenching agent for example by addition of acid, for example sulphuric acid and allowed to stand for a period of time, for example at least 1 hour, preferably 1 to 20 hours, for example overnight.
• a removal agent for example hydroxide and especially calcium hydroxide to remove salts of the reducing agent and quenching agent.
• the butanediol produced from the first portion is then contacted with the second portion of the ester of (R) 3-hydroxybutanoate.
• transesterificatioin is suitably carried out in the presence of a transesterification catalyst, for example an enzyme, acid or base.
• a transesterification catalyst for example an enzyme, acid or base.
• Suitable examples of enzymes include lipase
• suitable acids include mineral acids for example sulphuric acid and hydrochloric acid
• suitable bases include alkali metal hydroxides and alkali metal alkoxides.
• the transesterification reaction between the second portion and (R)-1 ,3- butanediol is carried out at elevated temperature, for example from 30 to 150 °C, particularly 40 to 100 °C.
• This transesterification process may be carried out in a batch or continuous process. Suitably the transesterification process is carried out for at least 1 hour, preferably 1 to 20 hours, for example 5 to 10 hours.
• the product of the reaction may then be subjected to further treatment to remove catalyst, unreacted starting materials and by-products, for example by filtering, distillation or the like.
• the invention will be illustrated by the following non-limiting examples.
• a 5 gallon Parr reactor is charged with 12.5L (10kg) 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 1 10°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.
• 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 I PA.
• 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.
• a heavy duty stainless steel stock pot is charged with 12L water and a portion of (3.49L) ethyl (R) 3-hydroxybutyraie. 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.
• 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 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.
• a solution is prepared by combining and mixing 600ml 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.

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• 2014
  • 2014-03-14 GB GB1404577.7A patent/GB2515603B/en not_active Expired - Fee Related
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  • 2014-03-14 DK DK14711210.6T patent/DK2984066T3/en active
  • 2014-03-14 WO PCT/EP2014/055156 patent/WO2014140308A1/en not_active Ceased
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