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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978085Generated: October 29, 2026

Hydrochloric Acid → 3-Hydroxy-2-(p-methoxyphenyl)-5-trifluoromethylbenzo[b]thiophene

https://huagongshe.com/reaction/978085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-(p-methoxybenzylthio)-5-trifluoromethylbenzoateHCID 20205034—
SolventDimethylformamideHCID 6228—
Product3-Hydroxy-2-(p-methoxyphenyl)-5-trifluoromethylbenzo[b]thiopheneHCID 20205020—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a mixture of sodium hydride (50% dispersion in mineral oil) (134 mg, 2.79 mmol) in N,N-dimethylformamide (3 ml) at 75° C. under a nitrogen atmosphere was added dropwise with stirring a solution of methyl 2-(p-methoxybenzylthio)-5-trifluoromethylbenzoate (500 mg, 1.40 mmol) in N,N-dimethylformamide (10 ml). After stirring 30 minutes at 75° C., the mixture was poured into water (50 ml), the mixture brought to pH5 with 2N hydrochloric acid, the product extracted with diethyl ether, the combined extracts washed with water, dried (sodium sulfate), and evaporated. The residue was chromatographed on a column of silica gel (Merck 7734, packed as a slurry in 25:1 hexane-ether). Elution with 25:1 hexane-ether containing 1% acetic acid afforded the desired product as a white solid upon evaporation of the appropriate fractions; yield 385 mg (85%); m/z 324 (M+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663344
Source datasetuspto-grants-1987_05
ORD IDord-3feef361eedd4a3a9a00a5a6d88a2783
Source noteuspto-grants-1987_05