Реакция #1178407

ord-687cb2135f9449fd9a912b0afafa338a

Уравнение реакции

O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
glucose
O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
glucose
CC(=O)c1ccccc1
acetophenone
[Na+].[OH-]
sodium hydroxide
C[C@H](O)c1ccccc1
(S)-phenylethanol
Выход 96.4%

Реагенты

Условия реакции

Температура
30°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ЭкстракцияThus, 100 mL of the cell-free extract
  2. 2
    Другоеwas produced
  3. 3
    workup.ADDITIONwas added dropwise to the mixture
  4. 4
    ДругоеAfter the reaction
  5. 5
    Экстракцияthe reaction mixture was extracted with toluene
  6. 6
    Сушкаwas dried over anhydrous sodium sulfate
  7. 7
    ДругоеRemoval of sodium sulfate, and evaporation of organic solvents from the organic layer

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08129163B2uspto-grants-2012_03