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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227126Generated: October 26, 2026

Decalin → HCID 22501123, compound

https://huagongshe.com/reaction/2227126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecalinHCID 7044—
Reactant1,4-DibromobenzeneHCID 7804—
ReactantPotassium HydroxideHCID 14797—
Reactant9H-Tribenzo[b,d,f]azepineHCID 11299519—
CatalystCopperHCID 23978—
SolventChloroformHCID 6212—
ProductHCID 22501123HCID 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 numberUS06413657B1
Source datasetuspto-grants-2002_07
ORD IDord-e3c9982081c44f9597bec9d3655c8635
Source noteuspto-grants-2002_07