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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637882Generated: October 31, 2026

Glycol monoethyl ether → 10,11-Dihydro-10-oxo-5H-dibenz(b,f)azepine-5-carbonitrile

https://huagongshe.com/reaction/637882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycol monoethyl etherHCID 8076—
Reactant10-Nitro-5H-dibenz(b,f)azepine-5-carbonitrileHCID 22467891—
CatalystIronHCID 23925—
SolventHydrochloric AcidHCID 313—
Product10,11-Dihydro-10-oxo-5H-dibenz(b,f)azepine-5-carbonitrileHCID 15895875—

Reaction Steps

26.3 g (0.1 mole) of 5-cyano-10-nitro-5H-dibenz[b,f]azepine are suspended in a mixture of 265 ml of ethylene glycol monoethyl ether and 75 ml of concentrated hydrochloric acid. 40 g of iron powder are added in small portions at 40° in the course of 40 minutes and the temperature is maintained at 40° by external cooling. The mixture is stirred for a further 2 hours at room temperature, is then heated to 80°, the precipitated product dissolving again, and is filtered through a heated suction filter, which is subsequently washed with ethylene glycol monoethyl ether. The crystallisation which commences in the filtrate is completed by adding 200 ml of water. After cooling for one hour in an ice-bath, filtration is carried out followed by washing with a mixture of ethylene glycol monoethyl ether and water in a ratio of 1:1. 5-cyano-10-oxo-10,11-dihydro-5H-dibenz[b,f]azepine is obtained which is identified, by comparing the IR spectra, with material from Example 27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559174
Source datasetuspto-grants-1985_12
ORD IDord-fca84d85f4874fa2aad14b383a198a72
Source noteuspto-grants-1985_12