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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219795Generated: October 27, 2026

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

https://huagongshe.com/reaction/219795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-(4-methyl-3-thienyl)-3-(trifluoromethyl)benzoateHCID 67528440—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(4-Methyl-3-thienyl)-3-(trifluoromethyl)benzoic acidHCID 5949581890.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of methyl 4-(4-methyl-3-thienyl)-3-(trifluoromethyl)benzoate (3 g; 9.99 mmol; 1 eq.) in EtOH (90 mL) at RT was treated with sodium hydroxide (5.99 mL; 5 M; 29.97 mmol; 3 eq.). The reaction mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated to give a brown solid which was taken up in water (300 mL) and the aqueous phase was washed twice with EtOAc. The aqueous phase was acidified with HCl cc to pH 2 and extracted with EtOAc (250 mL). The organic layer was dried over MgSO4 and concentrated affording the title compound as a brown oil (2.60 g, 90%). 1H NMR (DMSO-d6, 300 MHz) δ 13.07 (br s, 1H), 8.34-8.24 (m, 2H), 7.57-7.54 (m, 1H), 7.47-7.46 (m, 1H), 7.34-7.33 (m, 1H), 1.98 (s, 3H). LC/MS (Method A): 284.9 (M−H)−. HPLC (Method A) Rt 4.53 min (Purity: 95.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-c9a49ed059164e13bcd6b1ad8209bd71
Source noteuspto-grants-2012_06