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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589285Generated: October 25, 2026

Dimethylformamide → Methyl 7-(trifluoromethyl)-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/589285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl ThioglycolateHCID 16907—
Reactant2-Fluoro-3-(trifluoromethyl)benzaldehydeHCID 517978—
SolventWaterHCID 962—
ProductMethyl 7-(trifluoromethyl)-1-benzothiophene-2-carboxylateHCID 1852620389.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1.10 g of 2-fluoro-3-(trifluoromethyl)benzaldehyde, 663 mg of methyl thioglycolate, 1.03 g of potassium carbonate and 15 ml of DMF was stirred at 60° C. for 2 hours. 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 1.34 g of methyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09232792B2
Source datasetuspto-grants-2016_01
ORD IDord-30253522c6a04abe8c78526891c5ee3a
Source noteuspto-grants-2016_01