反应 #607440

ord-15b6b7f4129b4f74952914e02c45668f

反应方程式

CC(=O)c1cc(F)cc(F)c1
3′,5′-difluoroacetophenone
[BH4-].[Na+]
sodium borohydride
CC(O)c1cc(F)cc(F)c1
title compound
收率 99.3%
CC(O)c1cc(F)cc(F)c1
1-(3,5-difluorophenyl)ethanol
收率 99.3%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他quenched carefully by the addition of a saturated aqueous ammonium chloride solution (150 mL)
  2. 2
    萃取The extraction
  3. 3
    洗涤The combined organic layers were washed with brine (200 mL)
  4. 4
    干燥dried over anhydrous Na2SO4
  5. 5
    过滤filtered
  6. 6
    其他The solvent was removed in vacuo

实验过程

To a colorless stirred solution of 3′,5′-difluoroacetophenone (50.00 g, 320.24 mmol) in methanol (320 mL), sodium borohydride (3.41 g, 86.47 mmol, 0.27 eq) was added portion wise over 20 minutes at room temperature under inert atmosphere (Ar). Then the reaction mixture was stirred for 45 min at room temperature and then quenched carefully by the addition of a saturated aqueous ammonium chloride solution (150 mL). The extraction was carried out with ethyl acetate (2×200 mL). The combined organic layers were washed with brine (200 mL), dried over anhydrous Na2SO4 and filtered. The solvent was removed in vacuo to give the title compound (50.29 g, 99%) as a colorless oil. The alcohol was used as such in the subsequent step.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09326513B2uspto-grants-2016_05