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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271307Generated: October 30, 2026

Water → 5-(Trifluoromethyl)-1-benzothiophene-2-carboxylic acid

https://huagongshe.com/reaction/2271307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant5-Trifluoromethyl-benzo[b]thiophene-2-carboxylic acid methyl esterHCID 1477956—
SolventMethanolHCID 887—
Product5-(Trifluoromethyl)-1-benzothiophene-2-carboxylic acidHCID 278304396.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 10.0 g of methyl 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, 1.80 g of lithium hydroxide monohydrate, 30 ml of water and 90 ml of methanol was stirred at 75° C. for 1 hour. The reaction mixture was cooled to room temperature and then concentrated under reduced pressure. To the obtained residue was added water, and 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 9.10 g of 5-(trifluoromethyl)benzo[b]thiophene-2-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09119396B2
Source datasetuspto-grants-2015_09
ORD IDord-701126159e044d88a57218f1a9553e71
Source noteuspto-grants-2015_09