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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720221Generated: October 29, 2026

Phosphate → methyl (S)-4-bromo-3-hydroxybutyrate

https://huagongshe.com/reaction/720221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantNADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
ReactantSodium CarbonateHCID 10340—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantMethyl 4-bromo-3-oxobutanoateHCID 295655—
SolventButyl AcetateHCID 31272—
Productmethyl (S)-4-bromo-3-hydroxybutyrateHCID 11960268—

Reaction Conditions

Temperature30 °C

Reaction Steps

Methyl 4-bromo-3-oxobutyrate (300 mg), the above-mentioned wet bacterial cells (0.4 g), NADP+ (9 mg), glucose (750 mg), glucose dehydrogenase (manufactured by Amano Pharmaceuticals, Co., Ltd.) (1.2 mg), 100 mM phosphate buffer (pH 6.5) (15 ml) and butyl acetate (15 ml) are mixed. The mixture is stirred at 30° C. for 7 hr. During the stirring, 2M aqueous sodium carbonate solution is gradually added to adjust the pH of the reaction solution to 6.5±0.2. After the stirring has been finished, the reaction solution is centrifuged (1000×g, 5 min) to collect the organic layer. The organic layer is subjected to an analysis for content using gas chromatography under the following condition. The optical purity of methyl 4-bromo-3-hydroxybutyrate in the above-mentioned organic layer was also determined under the following condition. The organic layer was concentrated to give crude methyl (S)-4-bromo-3-hydroxybutyrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135318B2
Source datasetuspto-grants-2006_11
ORD IDord-ff304b25119448c08723d01c7943791e
Source noteuspto-grants-2006_11