Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566144Generated: October 31, 2026

Hydrochloric Acid → 7-Bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylic acid

https://huagongshe.com/reaction/566144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 7-bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylateHCID 18472216—
SolventSodium HydroxideHCID 14798—
SolventTetrahydrofuran ethanolHCID 21873804—
Product7-Bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylic acidHCID 18472517100%

Reaction Steps

In 1N sodium hydroxide (13.0 ml) and THF:ethanol (1:1, 50 ml) was dissolved ethyl 7-bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylate (2.77 g), and the mixture was stirred at room temperature for 15 hours. To the mixture was added 1N hydrochloric acid (12.5 ml), and the mixture was concentrated. To the residue was added water (200 ml), and the mixture was adjusted to pH 2 with 1N hydrochloric acid. The mixture was extracted with ethyl acetate(300 ml×3), and the organic layer was dried with magnesium sulfate. The solvent was evaporated under reduced pressure to give 7-bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylic acid (2.52 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-43915a424f4345c4b4584769d254a322
Source noteuspto-grants-2001_01