Reaction #2358486

ord-111c605a61134ec3ae46115e80cc1207

Reaction equation

O=Cc1ccc(C(F)(F)F)cc1F
2-fluoro-4-(trifluoromethyl)benzaldehyde
COC(=O)CS
methyl thioglycolate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CN(C)C=O
DMF
COC(=O)c1cc2ccc(C(F)(F)F)cc2s1
methyl-6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate
Yield 56.4%

Solvents

Conditions

Temperature
140°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturethe reaction mixture was cooled to room temperature
  2. 2
    Extractionextracted with tert-butyl methyl ether 3 times
  3. 3
    WashThe combined organic layer was washed with water
  4. 4
    DryingThe mixture was dried over magnesium sulfate
  5. 5
    Concentrationconcentrated under reduced pressure

Procedure

A mixture of 1.11 g of 2-fluoro-4-(trifluoromethyl)benzaldehyde, 739 mg of methyl thioglycolate, 1.3 g of potassium carbonate and 20 ml of DMF was stirred at 140° C. for 2 hours, and then the reaction mixture was cooled to room temperature. To the reaction mixture was added water, and then extracted with tert-butyl methyl ether 3 times. The combined organic layer was washed with water, followed by saturated aqueous sodium chloride solution. The mixture was dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 848 mg of methyl-6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate (the present compound 2).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09119396B2uspto-grants-2015_09