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
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-Chloro-2-ethylsulfanyl-6-methyl-benzonitrile | HCID 86699722 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Chloro-2-(ethylsulfinyl)-6-methyl-benzonitrile | HCID 86699727 | 37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108936B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-11c2f3c9e40f47c48acc4e2e06d6f468 |
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| Source note | uspto-grants-2015_08 |
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