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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271304Generated: October 30, 2026

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

https://huagongshe.com/reaction/2271304

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, 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09119396B2
Source datasetuspto-grants-2015_09
ORD IDord-111c605a61134ec3ae46115e80cc1207
Source noteuspto-grants-2015_09