反应 #1929034

ord-ad567422a364488a93e22265581bcba4

反应方程式

CC(=O)Cl
acetyl chloride
OCC(F)(F)F
trifluoroethanol
CCN(CC)CC
triethylamine
O
water
CC(=O)OCC(F)(F)F
2,2,2-trifluoroethyl acetate
收率 73.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    温度cooled
  3. 3
    其他was kept between 27° C. and 35° C
  4. 4
    workup.ADDITIONAfter that, the resultant mixed solution
  5. 5
    workup.STIRRINGwas stirred for 1.5 hours at room temperature
  6. 6
    其他Subsequently, an organic phase was separated by the reparatory funnel
  7. 7
    其他dried
  8. 8
    其他Thereafter, purification
  9. 9
    workup.DISTILLATIONby distilling

实验过程

85 g (0.85 mol) of trifluoroethanol and 80 ml of diethyl ether were poured to a separable flask of 1 liter, and further 129 g (1.27 mol/1.5 eq) of triethylamine was added thereto. Then, the resultant mixture was ice-cooled and stirred while dropping a solution diluting 100 g (1.27 mol/1.5 eq) of acetyl chloride with 80 ml of diethyl ether by dropping funnel. While dropping, the temperature of the solution was kept between 27° C. and 35° C. The period of time for dropping was 20 minutes. After that, the resultant mixed solution was stirred for 1.5 hours at room temperature and 350 ml of water was added, then, the reaction was completed. Subsequently, an organic phase was separated by the reparatory funnel and dried using magnesium sulfate. Thereafter, purification by distilling was conducted to obtain 88 g of 2,2,2-trifluoroethyl acetate of which yield was 73%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08945781B2uspto-grants-2015_02