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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282036Generated: November 3, 2026

Ethanethiol → 4-Bromo-2-methoxymethylbenzofuran-7-ol

https://huagongshe.com/reaction/1282036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-7-methoxy-2-methoxymethylbenzofuranHCID 18423639—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-methoxymethylbenzofuran-7-olHCID 1842365462.5%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a stirred solution of sodium hydride (334 mg, 60% in mineral oil) in dry N, N-dimethylformamide (25 ml) under an atmosphere of dry nitrogen at room temperature was added dropwise ethane thiol (0.586 ml). After stirring for 20 minutes a solution of 4-bromo-7-methoxy-2-methoxymethylbenzofuran (2.04 g) in N,N-dimethyl-formamide (7 ml) was added dropwise and the reaction mixture was heated at 160° C. for 2 hours. The reaction was cooled and the solvent removed in vacuo. The residue was dissolved in ethyl acetate (70 ml) and washed with ammonium chloride solution (70 ml). The organic extract was dried over magnesium sulphate, filtered and the solvent removed in vacuo. Purification by column chromatography on silica eluting with 50% ethyl acetate in hexane afforded the title compound as a white solid (1.21 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455561B1
Source datasetuspto-grants-2002_09
ORD IDord-f3cdf30459d24965b205b91934d3b310
Source noteuspto-grants-2002_09