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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515150Generated: October 29, 2026

m-Chloroperbenzoic acid → 4-Chloro-2-(ethylsulfinyl)-6-methyl-benzonitrile

https://huagongshe.com/reaction/515150

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-Chloro-2-ethylsulfanyl-6-methyl-benzonitrileHCID 86699722—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-2-(ethylsulfinyl)-6-methyl-benzonitrileHCID 8669972737%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-chloro-2-ethylsulfanyl-6-methyl-benzonitrile (synthesized according to the method described in section a) of example 2) (1.00 g, 4.73 mmol) in dichloromethane (20 ml) is added meta-chloroperoxybenzoic acid (0.58 g, 2.36 mmol, 70% suspension) portion wise at 0° C. The resulting mixture is stirred at 0° C. for 15 min. The white suspension is dissolved in ethyl acetate (25 ml) and the solvent is distilled off. The residue is again diluted with ethyl acetate (15 ml) and washed with 10% sodium sulphite solution (3×15 ml), saturated sodium hydrogen sulfate solution (3×15 ml), brine (15 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 8% ethyl acetate/hexane) to yield 4-chloro-2-(ethylsulfinyl)-6-methyl-benzonitrile (0.4 g, 1.76 mmol, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-11c2f3c9e40f47c48acc4e2e06d6f468
Source noteuspto-grants-2015_08