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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284225Generated: November 2, 2026

Benzoyl Peroxide → HCID 4534807, compound

https://huagongshe.com/reaction/1284225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22416519HCID 22416519—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 4534807HCID 4534807—

Reaction Steps

A mixture of 5-ethylidene-5H-dibenzo[a,d]cycloheptene (10.9 g., 0.05 mole), N-bromosuccinimide (8.9 g., 0.05 mole), benzoyl peroxide (15 mg.) and 150 ml. of carbon tetrachloride is stirred and heated to refluxing on the steam-bath for 4 hours. After cooling, the succinimide is separated by filtration and washed with carbon tetrachloride. The combined filtrate and washings are evaporated to dryness under reduced pressure. Crystallization of the residual solid from petroleum ether gave 5-(2-bromoethylidene)-5H-dibenzo[a,d]cycloheptene in a yield of 10.65 g. (72%), m.p. 87.5°-89.5°C. An analytical sample, after recrystallization from petroleum ether, melted at 89°-90°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978121
Source datasetuspto-grants-1976_08
ORD IDord-4ffcaabf41984b0582e4d968507bec10
Source noteuspto-grants-1976_08