Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464931Generated: October 30, 2026

HCID 13556875, compound → 8-Chloro-4,5-dihydro-1-phenyl-3H-2-benzazepine hydrochloride

https://huagongshe.com/reaction/464931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13556875HCID 13556875—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product8-Chloro-4,5-dihydro-1-phenyl-3H-2-benzazepine hydrochlorideHCID 13556878—

Reaction Steps

A solution of 5.1 g (12.6 mmole) of 1-[4-chloro-2-benzoylphenyl]-3-phthalimidopropane in 100 ml of ethanol and 20 ml of 3N sodium hydroxide was refluxed for 2 hr. The solution was diluted with 60 ml of 3N hydrochloric acid and refluxed for 12 hr. The mixture was diluted with water and extracted with ether. The aqueous layer was separated, made alkaline with dilute sodium hydroxide, and extracted with methylene chloride. The methylene chloride extract was dried over anhydrous sodium sulfate and concentrated at reduced pressure to dryness. The residue was purified by plug filtration (silica gel, 10 g; eluent, methylene chloride) and the eluent was acidified with methanolic hydrogen chloride. The solution was concentrated at reduced pressure to dryness and the residue was crystallized from a mixture of isopropanol and ether to give a colorless solid, mp 234°-235° C. Recrystallization from a mixture of methylene chloride and ether gave colorless needles, mp 234°-235° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04549988
Source datasetuspto-grants-1985_10
ORD IDord-fa7777c9d5a244d3933badd18e903767
Source noteuspto-grants-1985_10