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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776083Generated: November 1, 2026

Dimethylformamide → Methyl 6-(trifluoromethyl)-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/1776083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl ThioglycolateHCID 16907—
Reactant2-Fluoro-4-(trifluoromethyl)benzaldehydeHCID 522929—
SolventWaterHCID 962—
ProductMethyl 6-(trifluoromethyl)-1-benzothiophene-2-carboxylateHCID 1852620256.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

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. The reaction mixture was cooled down to room temperature. To the reaction mixture was added water, and the mixture was extracted with tert-butyl methyl ether three times. The combined organic layers were washed with water and saturated saline, and dried over magnesium sulfate, then, concentrated under reduced pressure, to obtain 848 mg of methyl 6-(trifluoromethyl)benzo[b]thiophene-2carboxylate (present condensed ring compound 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265251B2
Source datasetuspto-grants-2016_02
ORD IDord-be41325f571742ba84d855f4424e8a88
Source noteuspto-grants-2016_02