反応 #2358490

ord-acfe27147c714dbf9aa70e020235efe9

反応方程式

O=C(Cl)C(=O)Cl
oxalyl chloride
O=C(O)c1cc2cc(C(F)(F)F)ccc2s1
5-(trifluoromethyl)benzo[b]thiophene-2-carboxylic acid
CCOC(=O)c1cc2cc(C(F)(F)F)ccc2s1
ethyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate
収率 74.1%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooling
  2. 2
    温度under reflux
  3. 3
    濃縮concentrated under reduced pressure
  4. 4
    workup.ADDITIONTo the residue was added chloroform
  5. 5
    洗浄the organic layer was washed with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution
  6. 6
    乾燥dried over magnesium sulfate
  7. 7
    濃縮concentrated under reduced pressure

実験手順

Then, 254 mg of oxalyl chloride was added to a mixture of 400 mg of 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylic acid and 20 ml of ethanol while ice-cooling, and the mixture was stirred for 6 hours under reflux. The reaction mixture was cooled to room temperature, and then concentrated under reduced pressure. To the residue was added chloroform, and then the organic layer was washed with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 330 mg of ethyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate (the present compound 5).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09119396B2uspto-grants-2015_09