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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719075Generated: October 31, 2026

NADP nicotinamide-adenine-dinucleotide phosphate → Ethyl (3S)-4-chloro-3-hydroxybutanoate

https://huagongshe.com/reaction/719075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
SolventWaterHCID 962—
SolventButyl AcetateHCID 31272—
ProductEthyl (3S)-4-chloro-3-hydroxybutanoateHCID 701927787.4%

Reaction Steps

To a 100 mL vessel connected to an automatic titrater by a pH electrode and a feeding tube for addition of base was charged a solution of glucose (12. g) in water (30 mL). To this solution was charged ketoreductase SEQ ID NO: 42 (100 mg); 50 mg GDH SEQ ID NO: 66 and NADP (6.25 mg). Butyl acetate (10 ml) was then charged. Ethyl 4-chloroacetoacetate (10 g) was then charged via syringe pump as follows: 1 mL was charged rapidly and the remainder was then charged at a rate of 1 mL/hr). The pH was maintained at 7 by the automatic titrater by the addition of 4M NaOH over 18 hours hrs. The stirring was stopped and the phases allowed to separate. The organic layer included some emulsion. The organic layer, including some emulsion, was separated and washed with 10 mL of water. The combined aqueous layers were extracted twice with 20 mL of butyl acetate. The organic extracts were combined and rotary evaporated under vacuum to remove water. Additional butyl acetate was added during the evaporation to help remove the water. When the water was removed the butyl acetate solution was decanted from solids in the flask. Evaporation of the solvent under vacuum then gave 8.85 g of ethyl (S)-4-chloro-3-hydroxybutyrate (87.4% yield) of very good purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132267B2
Source datasetuspto-grants-2006_11
ORD IDord-c9da4ef4b56a4eef9f815df5982be991
Source noteuspto-grants-2006_11