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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109596Generated: October 29, 2026

Benzoyl Peroxide → HCID 14666741, compound

https://huagongshe.com/reaction/1109596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantTriethylamineHCID 8471—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 11024936HCID 11024936—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
ProductHCID 14666741HCID 14666741—

Reaction Steps

32 g of methyl 10-chloro-6,7-dihydro-4-oxo-3-phenyl-4H-benzo[a]quinolizine-1-carboxylate were heated under reflux for 16 hours in 350 ml of carbon tetrachloride with 16 g of N-bromosuccinimide in the presence of 280 mg of dibenzoyl peroxide. The mixture is left to cool and 24.3 ml of triethylamine were added thereto. The mixture was then again heated under reflux for 3 hours. After cooling, the mixture was treated with about 900 ml of methylene chloride, and the organic phase was washed once with 550 ml of 1N hydrochloric acid and thereafter dried over sodium sulfate, filtered and evaporated. The residue was purified by chromatography on silica gel and was recrystallized from ethyl acetate. There was obtained methyl 10-chloro-4-oxo-3-phenyl-4H-benzo[a]quinolizine-1-carboxylate as yellow crystals of m.p. 169°-170°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05321021
Source datasetuspto-grants-1994_06
ORD IDord-0d3a869ac2f7486b8d309338cf690eaf
Source noteuspto-grants-1994_06