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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | NADP nicotinamide-adenine-dinucleotide phosphate | HCID 5886 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | Ethanone, 2-chloro-1-(3-chlorophenyl)- | HCID 168006 | — |
| Product | 2-Chloro-1-(3-chloro-phenyl)-ethanol | HCID 11469563 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07332312B2 |
|---|
| Source dataset | uspto-grants-2008_02 |
|---|
| ORD ID | ord-45f69e5a8d054a9cb895e773c9c6a685 |
|---|
| Source note | uspto-grants-2008_02 |
|---|