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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38205Generated: October 29, 2026

Ethanol → 1-(Methylsulfinyl)-3-nitrobenzene

https://huagongshe.com/reaction/38205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuryl chlorideHCID 24648—
Reactant1-(Methylthio)-3-nitrobenzeneHCID 75656—
SolventDichloromethaneHCID 6344—
Product1-(Methylsulfinyl)-3-nitrobenzeneHCID 28029790.3%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of 3-nitro thioanisol (96 g, 568 mmol) in DCM (100 mL) was added dropwise to a cooled solution of sulfuryl chloride (96 g, 711 mmol) in DCM (600 mL) at −60° C. The mixture was stirred for 4 h at −20° C., then cooled to −60° C., and 350 mL of EtOH were carefully added. The reaction was then allowed to warm up to rt, subsequently, most of the solvent was evaporated, the residue was poured in sat. aq. NaHCO3, and the solid product was filtered off and carefully washed with hexane on the filter, then air-dried to give the desired sulfoxide (95 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524724B2
Source datasetuspto-grants-2013_09
ORD IDord-cb391335bab64dc3bd3bed1711b5ccd0
Source noteuspto-grants-2013_09