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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504575Generated: October 30, 2026

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

https://huagongshe.com/reaction/1504575

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-2-carboxylate (present condensed ring compound 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09215871B2
Source datasetuspto-grants-2015_12
ORD IDord-04402ee208c54390b135dee042494c2d
Source noteuspto-grants-2015_12