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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223744Generated: October 29, 2026

Ammonia → HCID 13055167, compound

https://huagongshe.com/reaction/223744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 20468881HCID 20468881—
SolventEthanolHCID 702—
ProductHCID 13055167HCID 13055167—

Reaction Steps

The solution of 5.4 g of 2-(o-bromomethylphenyl)-5-bromo-2'-fluorobenzophenone in 10 ml of ethanol is added slowly to the solution of 150 ml of saturated ethanolic ammonia while stirring at room temperature. After 2 days the mixture is evaporated, the residue taken up in methylene chloride and the solution washed with aqueous sodium carbonate. The organic layer is dried, evaporated and 5 g of the residue chromatographed on 50 g of silica gel, using first toluene, then toluene-diethyl ether (9:1) as the eluent. The later fraction is evaporated and the residue crystallized from hexane to yield the 9-bromo-7-(o-fluorophenyl)-5H-dibenz[c,e]azepine melting at 104°-105°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04356176
Source datasetuspto-grants-1982_10
ORD IDord-53caaee7a476410db3f9160d13984f3a
Source noteuspto-grants-1982_10