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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091225Generated: November 2, 2026

Acetophenone → 1-Phenylethanol, (S)-

https://huagongshe.com/reaction/1091225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantSodium HydroxideHCID 14798—
Reactant(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
CatalystNadide (JAN/USAN/INN)HCID 5893—
Product1-Phenylethanol, (S)-HCID 44313596.4%

Reaction Conditions

Temperature30 °C

Reaction Steps

coli HB101 (pNCM) was cultivated in a similar manner to Example 9, and then cells were disrupted with an ultrasonic homogenizer. Thus, 100 mL of the cell-free extract was produced. In a 100-mL portion of this cell-free extract, 700 U of a glucose dehydrogenase (Trade name: GLUCDH “Amano” II, a product of Amano Enzyme Inc.), 17 g of glucose, 3 mg of NAD+, and 10 g of acetophenone were added, and the mixture was stirred at 30° C. for 20 hours while controlling the pH of the reaction mixture to 6.5 with 5 N aqueous sodium hydroxide, which was added dropwise to the mixture. After the reaction, the reaction mixture was extracted with toluene, and combined organic layer was dried over anhydrous sodium sulfate. Removal of sodium sulfate, and evaporation of organic solvents from the organic layer yielded 9.8 g of (S)-phenylethanol. The product (S)-phenylethanol was analyzed in accordance with the [Analysis condition (1) for gas chromatography] as described above, and found that the optical purity of the product was 99.9% e.e. or higher.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129163B2
Source datasetuspto-grants-2012_03
ORD IDord-687cb2135f9449fd9a912b0afafa338a
Source noteuspto-grants-2012_03