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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508573Generated: October 28, 2026

7-Bromo-1,2,4,5-tetrahydro-3H-2-benzazepin-3-one → 7-Bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine hydrochloride

https://huagongshe.com/reaction/508573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Bromo-1,2,4,5-tetrahydro-3H-2-benzazepin-3-oneHCID 59015714—
Reactant7-Bromo-1,3,4,5-tetrahydro-2H-3-benzazepin-2-oneHCID 59015718—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine hydrochlorideHCID 12148829—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 1000-mL round-bottom flask was added the mixture of 7-bromo-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one and 7-bromo-1,2,4,5-tetrahydro-3H-2-benzazepin-3-one (12.6 g, 52.4 mmol) and tetrahydrofuran (260 mL). The solution was cooled to 0° C. and borane-methylsulfide complex (12.4 mL, 210 mmol) was slowly added. The reaction mixture was stirred at 0° C. for 10 min, warmed to room temperature and stirred for 3 h, then heated at reflux for 4 h. Upon cooling to room temperature, the mixture was quenched with MeOH (50 mL) to remove excess borane. The solvent was then evaporated to give 7-bromo-2,3,4,5-tetrahydro-1H-benzoazepine and 7-bromo-2,3,4,5-tetrahydro-1H-benzoazepine as sticky oil. LCMS: (FA) ES+ 226 and 228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096518B2
Source datasetuspto-grants-2015_08
ORD IDord-bdb4ce29037c4a868027c9525712c3a5
Source noteuspto-grants-2015_08