反応 #7067

ord-d146ffc4743f46cfb9a96289a70a2846

反応方程式

COS(=O)(=O)c1ccc(C)cc1
methyl p-toluenesulfonate
CCOC(=O)CC(=O)C(F)(F)F
ethyl 4,4,4-trifluoroacetoacetate
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCOC(=O)C=C(OC)C(F)(F)F
title compound
収率 56.0%
CCOC(=O)C=C(OC)C(F)(F)F
4,4,4-Trifluoro-3-methoxy-but-2-enoic acid ethyl ester
収率 56.0%

溶媒

反応条件

温度
70°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度After cooling to room temperature
  2. 2
    抽出extracted with Et2O (2×150 mL)
  3. 3
    洗浄washed with H2O and brine
  4. 4
    乾燥dried (Na2SO4)
  5. 5
    ろ過filtered
  6. 6
    濃縮concentrated

実験手順

To a solution of ethyl 4,4,4-trifluoroacetoacetate (12 mL, 82 mmol) in DMF (80 mL) is added cesium carbonate (26.4 g, 82 mmol). The reaction mixture is heated to 70° C. A solution of methyl p-toluenesulfonate (13.5 mL, 90 mmol) in DMF (30 mL) is then added dropwise during 30 min and the reaction mixture is stirred for an additional 1 hr. After cooling to room temperature, the reaction mixture is diluted with H2O (150 mL) and extracted with Et2O (2×150 mL). The organic extracts are combined and washed with H2O and brine, then dried (Na2SO4), filtered and concentrated to afford the title compound (9.0 g, 56%) as an oil which is used without further purification.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07084170B2uspto-grants-2006_08