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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586923Generated: October 26, 2026

Water → methyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate

https://huagongshe.com/reaction/586923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22328963—
SolventDimethylformamideHCID 6228—
Productmethyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22329080—

Reaction Conditions

Temperature45 °C

Reaction Steps

In DMF (3 ml) was dissolved methyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate (0.3 g), and the solution was added dropwise to a suspension of 60% sodium hydride (0.05 g) in DMF (1 ml) under ice-cooling. The mixture was stirred under nitrogen atmosphere for 10 minutes. Benzyl bromide (0.15 ml) was added thereto, and the mixture was heated at 45° C. for 4 hours. The mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried with anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified with silica gel column chromatography (ethyl acetate/hexane) to give methyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate (0.3 g) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-625f389470204eb499acabf1164a22ac
Source noteuspto-grants-2005_08