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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587089Generated: October 30, 2026

Chloride → methyl 7-bromo-1-(2-oxopropyl)-2,3-dihydro-1H-1-benzazepine-4-carboxylate

https://huagongshe.com/reaction/587089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantMethyl 1-allyl-7-bromo-2,3-dihydro-1-benzazepine-4-carboxylateHCID 11324721—
ReactantN,N-Dimethylformamide--water (1/1)HCID 21962138—
CatalystPalladium ChlorideHCID 24290—
SolventSodium chloride; waterHCID 57417360—
Productmethyl 7-bromo-1-(2-oxopropyl)-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22329093—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of palladium chloride (96 mg) and curious chloride (218 mg) in DMF-water (7-1 ml) was stirred at 60° C. for 18 hours under oxygen atmosphere. To the reaction system was added a solution of methyl 7-bromo-1-(2-propenyl)-2,3-dihydro-1H-1-benzazepine-4-carboxylate (500 mg) in DMF-water (7-1 ml) was added, and the mixture was stirred at 60° C. for 7 hours. To the reaction system was added saturated brine, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate. After concentration under reduced pressure, the residue was separated and purified with column chromatography (ethyl acetate:hexane=1:4→1:2) to give methyl 7-bromo-1-(2-oxopropyl)-2,3-dihydro-1H-1-benzazepine-4-carboxylate (311 mg) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-d62baa39a8034789a8c9b053dec03673
Source noteuspto-grants-2005_08