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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227127Generated: October 26, 2026

Decalin → 5-(4-(2-hydroxyethyl)phenyl)-5H-dibenz[b,f]azepine

https://huagongshe.com/reaction/2227127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecalinHCID 7044—
ReactantDibenz(b,f)azepineHCID 9212—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(4-Iodophenyl)ethan-1-olHCID 3040770—
CatalystCopperHCID 23978—
SolventChloroformHCID 6212—
Product5-(4-(2-hydroxyethyl)phenyl)-5H-dibenz[b,f]azepineHCID 1300824830%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 8.7 g (45 mmol) of 5H-dibenz[b,f]azepine, 12.4 g (50 mmol) of p-iodophenethyl alcohol, 2.8 g (50 mmol) of potassium hydroxide, 4.8 g (75 mmol) of copper powder, and 20 ml of decalin was heated at an external temperature of 200° C. while stirring in a nitrogen stream for 40 hours. The reaction mixture was cooled nearly to room temperature, chloroform was added thereto, followed by filtration using Celite to remove any insoluble matter. The filtrate was concentrated. To remove decalin, n-hexane was added to the residue, followed by filtration. The filter cake was reprecipitated in methanol, and the resulting crude product was purified by silica gel column chromatography to give 4.2 g (30%) of 5-(4-(2-hydroxyethyl)phenyl)-5H-dibenz[b,f]azepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413657B1
Source datasetuspto-grants-2002_07
ORD IDord-43be315c48004880a214528c539fd109
Source noteuspto-grants-2002_07