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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589281Generated: October 30, 2026

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

https://huagongshe.com/reaction/589281

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09232792B2
Source datasetuspto-grants-2016_01
ORD IDord-0247623088074d76875e4ab95f35e7c3
Source noteuspto-grants-2016_01