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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277317Generated: November 2, 2026

Hydrochloric Acid → Ethyl 7-bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylate

https://huagongshe.com/reaction/1277317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactantethyl 4-(4-bromo-2,N-diformylanilino)butyrateHCID 21715711—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductEthyl 7-bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylateHCID 1847221622%
Product7-Bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylic acidHCID 1847251710%

Reaction Steps

In t-butanol (500 ml) were dissolved ethyl 4-(4-bromo-2,N-diformylanilino)butyrate (15.32 g) and potassium t-butoxide (5.53 g), and the mixture was ref luxed for 30 minutes. To the mixture were added water (500 ml) and 1N hydrochloric acid (50 ml), and the mixture was extracted with ethyl acetate (1000 ml). Theorganiclayerwaswashedwithsaturatedbrine (200 ml) and dried with magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified with silica gel column chromatography (300 g, hexane:ethyl acetate=4:1→1:1) to give ethyl 7-bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylate (3.13 g, 22%) and 7-bromo-1-formyl-2,3-dihydro-1-benzazepine-4-carboxylic acid (1.39 g, 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-736d4569bdeb4b27a0646c1e45fe27f9
Source noteuspto-grants-2000_12