HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712871Generated: October 30, 2026
NADP nicotinamide-adenine-dinucleotide phosphate → 1,1-Dimethylethyl N-[(1S,2R)-3-chloro-2-hydroxy-1-(phenylmethyl)propyl]carbamate
https://huagongshe.com/reaction/1712871
Participants
| Role | Name | HCID | Charge |
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| 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 | tert-butyl N-((2S)-4-chloro-3-oxo-1-phenylbutan-2-yl)carbamate | HCID 9926241 | — |
| Product | 1,1-Dimethylethyl N-[(1S,2R)-3-chloro-2-hydroxy-1-(phenylmethyl)propyl]carbamate | HCID 9944139 | 86.3% |
Reaction Steps
Glucose dehydrogenase (manufactured by Amano Enzyme) 2000 U, glucose 2 g, NADP 6 mg, (3S)-1-chloro-3-tert-butoxycarbonylamino-4-phenyl-2-butanone 2.5 g were added to 50 ml of a cell-free extract of E. coli HB101 (pNTOM3) prepared in Example 7, and the mixture was stirred at 30° C. for 22 hr while adjusting to pH 6.5 by dropwise addition of 5 M sodium hydroxide. After completion of the reaction, the reaction mixture was extracted with toluene, desolvated and the extract was analyzed. As a result, (2R,3S)-1-chloro-3-tert-butoxycarbonylamino-4-phenyl-2-butanol (yield 86.3%, diastereomeric excess 96.4% d.e.) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07794993B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-0e561c086a114001bcd188f1a146b0a5 |
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| Source note | uspto-grants-2010_09 |
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