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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587022Generated: November 1, 2026

Benzoyl Peroxide → HCID 86746917, compound

https://huagongshe.com/reaction/1587022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 86746915HCID 86746915—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 86746917HCID 86746917—

Reaction Steps

A mixture of 3α, 12α-diacetoxy-17β-[(1,1-diphenyl)-1-penten-4-yl]-5β-androstane (7.24 g), N-bromosuccinimide (2.26 g) and benzoyl peroxide (0.256 g) in anhydrous carbon tetrachloride (250 ml) is stirred at reflux, while being illuminated with a 275-watt sun lamp, for about 45 minutes. The mixture is cooled, filtered, and concentrated in vacuo. The resulting oil is dissolved in anhydrous pyridine (12.2 ml), the solution refluxed for about 1 hour, and concentrated in vacuo. The residue is dissolved in ether, filtered, and the ether solution washed with dilute sodium chloride solution, dried over magnesium sulfate, filtered and concentrated in vacuo. The crude product is used, without further treatment, for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05216015
Source datasetuspto-grants-1993_06
ORD IDord-4fff185621144e65882a941b449b5603
Source noteuspto-grants-1993_06