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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35173Generated: October 27, 2026

Cyanogen Bromide → 5,7-dihydro-6H-dibenz[c,e]azepine-6carbonitrile

https://huagongshe.com/reaction/35173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant5H-Dibenz(c,e)azepine, 6,7-dihydro-HCID 81183—
SolventChloroformHCID 6212—
Product5,7-dihydro-6H-dibenz[c,e]azepine-6carbonitrileHCID 19833886—

Reaction Steps

A solution of 1.91 g of cyanogen bromide in 20 ml of chloroform is added dropwise at 5°-10° C. within 25 minutes to a solution, cooled to 5° C., of 7 g of 6,7-dihydro-5H-dibenz[c,e]azepine in 50 ml of chloroform. The reaction mixture is stirred for a further 1 hour and then a small amount of the hydrobromide salt of the still unreacted azepine is filtered off. The filtrate is washed three times with water, dried over anhydrous sodium sulphate and evaporated. There is obtained solid 5,7-dihydro-6H-dibenz[c,e]azepine-6-carbonitrile, m.p. 123°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766115
Source datasetuspto-grants-1988_08
ORD IDord-ec01c07dd42e42d19e85933e8284aee8
Source noteuspto-grants-1988_08