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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968855Generated: November 1, 2026

m-Chloroperbenzoic acid → N-[3-(3-Formyl-4-nitro-benzenesulfinyl)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/1968855

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[3-(3-Formyl-4-nitro-phenylsulfanyl)-phenyl]-benzenesulfonamideHCID 58625048—
SolventChloroformHCID 6212—
ProductN-[3-(3-Formyl-4-nitro-benzenesulfinyl)-phenyl]-benzenesulfonamideHCID 58625065—

Reaction Steps

A mixture of N-[3-(3-formyl-4-nitro-phenylsulfanyl)-phenyl]-benzenesulfonamide (0.0034 mol) and 3-Chloro-benzenecarboperoxoic acid (also known as MCPBA or meta-chloroperbenzoic acid) (0.7 g; 75%) in CHCl3 (q.s.) was stirred for 4 hours at room temperature. Then a NaHCO3 solution was added, and the reaction mixture was stirred. The organic layer was separated, dried, and filtered, and the solvent was evaporated. The residue was purified by column chromatography over Biotage (gradient eluent: CH2Cl2:CH3OH). The purest product fractions were collected, and the solvent was evaporated to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426429B2
Source datasetuspto-grants-2013_04
ORD IDord-fe41121cb519480f9c1834b878c0aa5b
Source noteuspto-grants-2013_04