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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904823Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 14013348, compound

https://huagongshe.com/reaction/1904823

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 14013331HCID 14013331—
SolventDichloromethaneHCID 6344—
ProductHCID 14013348HCID 140133489%

Reaction Steps

To a stirred and cooled (0° C.) mixture of 7.2 parts of 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]thio]-1-[(4-methylphenyl)sulfonyl]piperidine and 95 parts of dichloromethane was added dropwise a solution of 2.6 parts of 3-chlorobenzenecarboperoxoic acid in dichloromethane. Upon completion, stirring was continued for 2 hours at room temperature. The reaction mixture was washed with a sodium carbonate solution and with water. The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (96:4 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 0.7 parts (9%) of 4-[[1-[(4-fluorophenyl)methyl]1H-benzimidazol-2-yl]sulfinyl]-1-[(4-methylphenyl)sulfonyl]piperidine; mp. 166.2° C. (30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839374
Source datasetuspto-grants-1989_06
ORD IDord-68b24b0d0665490fa01911c2e5b2a7e4
Source noteuspto-grants-1989_06