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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504576Generated: October 29, 2026

Dimethylformamide → Methyl 4-(trifluoromethyl)-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/1504576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl ThioglycolateHCID 16907—
Reactant2-Fluoro-6-(trifluoromethyl)benzaldehydeHCID 521933—
SolventWaterHCID 962—
ProductMethyl 4-(trifluoromethyl)-1-benzothiophene-2-carboxylateHCID 1852620135.4%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 1.00 g of 2-fluoro-6-(trifluoromethyl)benzaldehyde, 633 mg of methyl thioglycolate, 1.21 g of potassium carbonate and 15 ml of DMF was stirred at 130° 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 480 mg of methyl 4-(trifluoromethyl)benzo[b]thiophene-2-carboxylate (present condensed ring compound 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09215871B2
Source datasetuspto-grants-2015_12
ORD IDord-049c933fb52e49a58938bbb9be9b27a1
Source noteuspto-grants-2015_12