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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358045Generated: October 30, 2026

Bromine → HCID 22105454, compound

https://huagongshe.com/reaction/358045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantHCID 20449988HCID 20449988—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 22105454HCID 22105454—

Reaction Steps

A suspension of 10.25 g of 7-chloro-5-(2-fluorophenyl)-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one in 880 ml of carbon tetrachloride is treated with 4.5 ml of bromine and heated to boiling while stirring for 2 hours while irradiating with a 500 W incandescent lamp. The solution is evaporated in vacuo. The residue is dissolved in 880 ml of 2 propanol and hydrogenated at room temperature and normal pressure in the presence of 1.3 g of palladium-on-carbon (5%). The catalyst is filtered off and the filtrate is evaporated. The residue is dissolved in benzene and chromatographed on 295 g of silica gel. Impurities and starting material are eluted with benzene/ethyl acetate (29:1) and the desired product is eluted with benzene/ethyl acetate (19:1). After recrystallization from benzene/ether, there is obtained 7-chloro-5-(2-fluorophenyl)-1,3-dihydro-2H-1-benzazepin-2-one of melting point 214°-215°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464300
Source datasetuspto-grants-1984_08
ORD IDord-fd50aca8ac42475f91ba9da37aef7f48
Source noteuspto-grants-1984_08