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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648856Generated: October 31, 2026

Benzoyl Peroxide → HCID 14153223, compound

https://huagongshe.com/reaction/648856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-[(dimethylamino)sulfonyl]-2-methylbenzoateHCID 13937642—
SolventDiethyl EtherHCID 3283—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 14153223HCID 14153223—

Reaction Steps

A mixture of 25.7 g of the product from Example 10, 17.8 g of N-bromosuccinimide, and 1.0 g benzoyl peroxide in 350 ml carbon tetrachloride was stirred at reflux temperature for 3.5 hours and then at room temperature overnight. The by-product succinimide was removed by filtration and the filtrate concentrated in vacuo to afford an oil which was dissolved in ether and washed with two portions of water. Drying and evaporation of the ether layer afforded a viscous yellow oil which was shown by 1H NMR analysis to consist of the title compound and unreacted starting material in a ratio of approximately 2:1. This mixture was carried directly on to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737185
Source datasetuspto-grants-1988_04
ORD IDord-5baf883a48694dc7a2b98e617f92323f
Source noteuspto-grants-1988_04