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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354464Generated: October 30, 2026

Hydrochloric Acid → [5-(4-Trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoic acid

https://huagongshe.com/reaction/1354464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-[5-(4-trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoateHCID 22934538—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product[5-(4-Trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoic acidHCID 2110576383%

Reaction Steps

A mixture of methyl 4-[5-(4-trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoate (0.838 g), 1 M aqueous sodium hydroxide solution (5 ml), tetrahydrofuran (100 ml) and methanol (50 ml) was heated under reflux for 1 hr. After cooling, the reaction mixture was poured into water, and 1 M hydrochloric acid was added to acidify the mixture. The mixture was extracted with ethyl acetate-tetrahydrofuran (1:1, volume ratio). The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was recrystallized from tetrahydrofuran to give 4 [5-(4-trifluoromethylphenyl)-1,3,4-thiadiazol-2-yl]benzoic acid (0.672 g, yield 83%) as a colorless crystalline powder. melting point: >300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223791B2
Source datasetuspto-grants-2007_05
ORD IDord-438ff29fa68b4c3db8d91591c939af7d
Source noteuspto-grants-2007_05