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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589286Generated: October 30, 2026

Water → 7-(Trifluoromethyl)-1-benzothiophene-2-carboxylic acid

https://huagongshe.com/reaction/589286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 7-(trifluoromethyl)-1-benzothiophene-2-carboxylateHCID 18526203—
SolventMethanolHCID 887—
Product7-(Trifluoromethyl)-1-benzothiophene-2-carboxylic acidHCID 1797962383.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 800 mg of methyl 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, 154 mg of lithium hydroxide monohydrate, 4 ml of water and 12 ml of methanol was stirred at 75° C. for 2 hours. The reaction mixture was cooled to room temperature, and then concentrated under reduced pressure. To the residue was added water, and then washed with tert-butyl methyl ether 3 times. To the aqueous layer was added concentrated hydrochloric acid, and then extracted with tert-butyl methyl ether 3 times. The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 632 mg of 7-(trifluoromethyl)benzo[b]thiophene-2-carboxylic acid (the present compound 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09232792B2
Source datasetuspto-grants-2016_01
ORD IDord-64ea382c66a94c9d837d6c641bcc757d
Source noteuspto-grants-2016_01