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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358427Generated: October 31, 2026

m-Chloroperbenzoic acid → Dimethylamine

https://huagongshe.com/reaction/358427

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 20447671HCID 20447671—
SolventChloroformHCID 6212—
ProductDimethylamineHCID 674—
ProductHCID 20447675HCID 20447675—

Reaction Steps

5.4 g of metachlorperbenzoic acid was added to a chloroform solution of 3.7 g of N-allyl-N-(α-methylbenzyl)-4-(N,N-dimethylcarbamoyl)benzenesulfonamide obtained by reaction between dimethylamine and N-allyl-N-(α-methylbenzyl)-4-chlorocarbonylbenzenesulfonamide. The mixture was reacted under reflux for 2 hours. Thereafter, an aqueous sodium sulfite solution was added to decompose the excess of the peroxide. After washing with an aqueous sodium bicarbonate solution and water, the chloroform solution was dried over anhydrous magnesium sulfate, concentrated and purified by the silica gel chromatography to obtain 3.0 g (77%) of the intended product (Compound No. 163), m.p. 98.0°~100.0° C. The elemental analysis of the product was effected with the results shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468245
Source datasetuspto-grants-1984_08
ORD IDord-708c6caf31844ca39ca0c9440f9e5a12
Source noteuspto-grants-1984_08