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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586833Generated: October 26, 2026

Hydrochloric Acid → Methyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate

https://huagongshe.com/reaction/586833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22329270HCID 22329270—
SolventEthyl AcetateHCID 8857—
ProductMethyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 2232896390.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

In ethyl acetate (50 ml) was dissolved methyl 7-bromo-1-(t-butoxycarbonyl)-2,3-dihydro-1H-1-benzazepine-4-carboxylate (1.5 g). To the solution was added 6N hydrochloric acid (2 ml), and the mixture was heated to stir at 80° C. for 2 hours, neutralized with 1N sodium hydroxide solution 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 to give methyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate (1.0 g) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-9d37eefaa9f248b6b2a0bcd0c35b94d2
Source noteuspto-grants-2005_08