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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719071Generated: November 2, 2026

Sodium Chloride → Ethyl (3S)-4-chloro-3-hydroxybutanoate

https://huagongshe.com/reaction/719071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantNADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
SolventButyl AcetateHCID 31272—
ProductEthyl (3S)-4-chloro-3-hydroxybutanoateHCID 701927797%

Reaction Steps

To a well-stirred solution of 100 mM potassium phosphate buffer, 500 mM NaCl, pH 7 (1 L) at room temperature was added glucose (160 g, 830 mmoles, 1.1 equiv). To this was added ketoreductase SEQ ID NO: 2 (0.9 g), glucose dehydrogenase S06 SEQ ID. NO: 10 (0.5 g) and NADP (0.5 g) as lyophilized powders. Once dissolved, butyl acetate (500 mL) was added to form an emulsion. To this emulsion was added a solution of ethyl 4-chloroacetoacetate (100 g, 608 mmoles) in butyl acetate (500 mL), dropwise over 3 hours. The pH was maintained between 6.8 and 7 by an automatic titrater that dispensed Na2CO3 (2M in water, about 160 mL total). After 40 hours the automated addition of the base had ceased and there was no residual starting material by gas chromatography. The layers were separated, and the aqueous phase was washed with ethyl acetate (500 mL). The combined organics were dried over anhydrous sodium sulfate, filtered and evaporated on a rotary evaporator, to give essentially pure (˜97%) ethyl (S)-4-chloro-3-hydroxybutyrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132267B2
Source datasetuspto-grants-2006_11
ORD IDord-a16bd48e0f614728896460969bee8c95
Source noteuspto-grants-2006_11