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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676200Generated: October 30, 2026

Methanesulfinic acid → 4-Bromo-1-(methanesulfonyl)-2-methylbenzene

https://huagongshe.com/reaction/1676200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfinic acidHCID 87251—
Reactant5-Bromo-2-iodotolueneHCID 2724601—
ReactantSodiumHCID 5360545—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product4-Bromo-1-(methanesulfonyl)-2-methylbenzeneHCID 20616765—

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 4-bromo-1-iodo-2-methylbenzene (240 μL, 1.68 mmol, Aldrich), Copper(I) iodide (353 mg, 1.85 mmol, Alfa Aesar), Methanesulfinic acid, sodium salt (688 mg, 6.74 mmol, Alfa Aesar) and DMSO (7.2 mL) was purged with Argon and then heated under microwave condition at 125° C. for 20 min. The resulting mixture was stirred at 100° C. for 3 h and then cooled to room temperature. The reaction mixture was diluted with H2O and extracted with EtOAc (2×). The organic layers were combined and washed with brine, dried over Na2SO4 and concentrated in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 0-50% EtOAc in hexanes) to yield 270 mg of desired product as a white solid. MS (ESI) 249 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003796B2
Source datasetuspto-grants-2011_08
ORD IDord-9216477e97a04b4cb160f648e08df23c
Source noteuspto-grants-2011_08