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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710466Generated: October 25, 2026

Oxalyl chloride → 6-Methoxy-1-benzothiophene-2,3-dione

https://huagongshe.com/reaction/1710466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-MethoxybenzenethiolHCID 84989—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDiethyl EtherHCID 3283—
Product6-Methoxy-1-benzothiophene-2,3-dioneHCID 344084847.4%

Reaction Steps

To a solution of 3-methoxythiophenol (3.75 g, 26.7 mmol) in ether (20 mL) was added oxalyl chloride (3.7 mL, 43 mmol) dropwise. The mixture was heated at reflux for 1.5 h, cooled to rt, and concentrated in vacuo. The resulting yellow oil was dissolved in dichloromethane (50 mL), cooled to 0° C., and was treated with aluminum chloride (4.30 g, 32.0 mmol) in portions. The mixture was heated at reflux for 30 min, cooled to rt, and poured onto ice water with stirring. The organic layer was separated and successively washed with saturated, aqueous sodium bicarbonate, water, and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (4/1 ethyl acetate/hexane) which provided 2.46 g (47%) of 6-methoxy-1-benzothiophene-2,3-dione as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790722B2
Source datasetuspto-grants-2010_09
ORD IDord-ea84e6025bfc44869b4bb1eac1393b9c
Source noteuspto-grants-2010_09