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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055066Generated: October 25, 2026

NADP nicotinamide-adenine-dinucleotide phosphate → 2-Chloro-1-(3-chloro-phenyl)-ethanol

https://huagongshe.com/reaction/2055066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
ReactantSodium HydroxideHCID 14798—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ReactantEthanone, 2-chloro-1-(3-chlorophenyl)-HCID 168006—
Product2-Chloro-1-(3-chloro-phenyl)-ethanolHCID 1146956396%

Reaction Conditions

Temperature30 °C

Reaction Steps

The culture of the recombinant Escherichia coli HB101(pNTRG) as obtained in Example 8 was subjected to ultrasonic cell disruption using SONIFIRE 250 (product of BRANSON). To 20 ml of this cell disruption fluid, there were added 2,000 U of glucose dehydrogenase (product of Amano Pharmaceutical Co., Ltd.), 3 g of glucose, 2 mg of NADP and 2 g of 2-chloro-1-(3′-chlorophenyl)ethanone. This reaction mixture was stirred at 30° C. for 18 hours while adjusting the pH to 6.5 by addition of 5 M sodium hydroxide. After completion of the reaction, this reaction mixture was extracted with toluene, the solvent was then removed, and the extract was analyzed. 2-Chloro-1-(3′-chlorophenyl)ethanol was obtained in 96% yield. The 2-chloro-1-(3′-chlorophenyl)ethanol formed on that occasion was the R form with an optical purity of 99.9% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332312B2
Source datasetuspto-grants-2008_02
ORD IDord-45f69e5a8d054a9cb895e773c9c6a685
Source noteuspto-grants-2008_02