Реакция #3105

ord-8461c7f0620f4c95ae6a995e75ca2bad

Уравнение реакции

CC(=O)OC1C=Cc2ccccc21
racemic 1-acetoxyindene
CC(C)=O
acetone
CC(=O)O[C@H]1C=Cc2ccccc21
(S)-1-acetoxyindene
Выход 44.6%
O[C@@H]1C=Cc2ccccc21
(R)-inden-1-ol
Выход 46.1%

Реагенты

Нет

Растворители

Условия реакции

Температура
37°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe reaction solution was filtered on Celite
  2. 2
    Другоеto remove lipase
  3. 3
    ЭкстракцияThe liltrate was extracted with diethyl ether
  4. 4
    Другоеthe extracted solution was dried on magnesium sulfate
  5. 5
    ДругоеThe solvent was removed under a reduced pressure

Методика

1.0 g (5.75 mmol) of racemic 1-acetoxyindene and 57.5 mg of lipase PS (made by Amano Seiyaku Sha, derived from Pseudomonas bacterium) were suspended in 58 ml of phosphate buffer (0.1M)-acetone mixed solution (9:1 V/V) and stirred at 37° C. for 48 hours. The reaction solution was filtered on Celite to remove lipase. The liltrate was extracted with diethyl ether and the extracted solution was dried on magnesium sulfate. The solvent was removed under a reduced pressure and the residue was subjected to silica gel column chromatography (eluate:ethyl acetate-hexane, 1:10 V/V) to separate into 446 mg (yield 44.6%) of (S)-1-acetoxyindene and 350 mg (yield 46.1%) of (R)-inden-1-ol respectively. The specific rotations and optical purities thereof were as shown below. The optical purities were determined by high speed liquid chromatography (column: chiral cell OD, eluate: isopropanol-hexane, 1% V/V).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05731464uspto-grants-1998_03