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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815609Generated: October 26, 2026

Decalin → 9-(4-bromophenyl)-9H-tribenz[b,d,f]azepine

https://huagongshe.com/reaction/1815609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecalinHCID 7044—
Reactant1,4-DibromobenzeneHCID 7804—
ReactantPotassium HydroxideHCID 14797—
Reactant9H-Tribenzo[b,d,f]azepineHCID 11299519—
CatalystCopperHCID 23978—
SolventChloroformHCID 6212—
Product9-(4-bromophenyl)-9H-tribenz[b,d,f]azepineHCID 2250112325.1%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 9.2 g (38 mmol) of 9H-tribenz[b,d,f]azepine (synthesized in accordance with J. Org. Chem., vol. 56, p. 3906 (1991)), 44.8 g (190 mmol) of 1,4-dibromobenzene, 5.6 g (100 mmol) of potassium hydroxide, 1.6 g (25 mmol) of copper powder, and 50 ml of decalin was heated at an external temperature of 200° C. for 36 hours in a nitrogen stream while stirring. The reaction mixture was cooled nearly to room temperature, chloroform was added thereto, followed by filtration using Celite to remove the insoluble matter. The filtrate was concentrated. To remove decalin, n-hexane was added to the residue, followed by filtration. The filter cake was purified by silica gel column chromatography to give 3.8 g (25%) of 9-(4-bromophenyl)-9H-tribenz[b,d,f]azepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878822B2
Source datasetuspto-grants-2005_04
ORD IDord-7e41dd52db1546d18fce8801b8f4c230
Source noteuspto-grants-2005_04