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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230884Generated: October 31, 2026

Hydrochloric Acid → 4-Methoxy-3-(2-phenylethyl)benzo[b]thiophene

https://huagongshe.com/reaction/230884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Carboxy-4-methoxy-3-(2-phenylethyl)benzo[b]thiopheneHCID 23103520—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
Product4-Methoxy-3-(2-phenylethyl)benzo[b]thiopheneHCID 2310351189.6%

Reaction Steps

A suspension of 2-carboxy-4-methoxy-3-(2-phenylethyl)benzo[b]thiophene (1 g) and a catalytic amount of copper powder in quinoline (15 mL) was stirred at 200° C. for 2 hours. The reaction mixture was cooled to room temperature and poured into 1 mol/L hydrochloric acid, and the resulting mixture was extracted with ethyl acetate. The extract was washed with 1 mol/L hydrochloric acid and water, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=5/1) to give the title compound (0.77 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566699B2
Source datasetuspto-grants-2009_07
ORD IDord-50415b8d3c7d4c0d81ff32d21763ee6f
Source noteuspto-grants-2009_07