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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950823Generated: October 31, 2026

Sodium Hydroxide → 4-(4-Methyl-3-thienyl)-3-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1950823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-(4-methyl-3-thienyl)-3-(trifluoromethyl)benzoateHCID 67528440—
SolventEthanolHCID 702—
Product4-(4-Methyl-3-thienyl)-3-(trifluoromethyl)benzoic acidHCID 5949581891%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydroxide (5M: 6 mL; 30 mmol; 3 eq.) was added to a solution of methyl 4-(4-methyl-3-thienyl)-3-(trifluoromethyl)benzoate (3 g; 10 mmol; 1 eq.) in EtOH (90 mL) and the reaction mixture was stirred at 60° C. for 2 hours. After evaporation of the solvent, the residue was taken up in water (300 mL) and the aqueous phase was washed with ethyl acetate (2×100 mL) then acidified to pH 2 with conc. HCl. The solution was concentrated to ca. 100 mL and extracted with ethyl acetate. The organic layer was dried over magnesium sulphate and concentrated in vacuo to afford the title compound (2.6 g, 91%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404676B2
Source datasetuspto-grants-2013_03
ORD IDord-b525ced19acf4ae794332aa8ae082d18
Source noteuspto-grants-2013_03