Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390282Generated: October 31, 2026

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

https://huagongshe.com/reaction/390282

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 numberUS08383637B2
Source datasetuspto-grants-2013_02
ORD IDord-b94f8f251a6346b59f0fccc1853d5f0a
Source noteuspto-grants-2013_02