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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-Bromo-1,2,4,5-tetrahydro-3H-2-benzazepin-3-one | HCID 59015714 | — |
| Reactant | 7-Bromo-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one | HCID 59015718 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine hydrochloride | HCID 12148829 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096518B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-bdb4ce29037c4a868027c9525712c3a5 |
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| Source note | uspto-grants-2015_08 |
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