Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815610Generated: October 26, 2026

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

https://huagongshe.com/reaction/1815610

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 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 numberUS06878822B2
Source datasetuspto-grants-2005_04
ORD IDord-6f51176524f446d89081b4557b98c0a5
Source noteuspto-grants-2005_04