HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540305Generated: October 30, 2026
(Dimethyl sulfide)trihydroboron → 7-Bromo-2,3,4,5-tetrahydro-1H-2-benzazepine
https://huagongshe.com/reaction/540305
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | 7-Bromo-1,2,4,5-tetrahydro-3H-2-benzazepin-3-one | HCID 59015714 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 7-Bromo-2,3,4,5-tetrahydro-1H-2-benzazepine | HCID 53397004 | 13.9% |
Reaction Steps
To a solution of 7-bromo-1,2,4,5-tetrahydro-3H-2-benzazepin-3-one (35 g, 146 mmol) in 1,2-dimethoxyethane (400 mL) was added a solution of borane dimethyl sulfide complex (1.0 M in tetrahydrofuran, 40 mL) under nitrogen and the resulting mixture was stirred under reflux overnight. The reaction was quenched with methanol, acidified with 2 M hydrochloric acid and then stirred for further 2 hours. The resulting mixture was concentrated in vacuo and the residue was purified by preparative HPLC to give 4.6 g of product. MS obsd. (ESI+) [(M+H)+] 226. 1H NMR (400 MHz, CDCl3) δ ppm 7.21 (d, J=5 Hz, 1 H), 7.15-7.13 (dd, J=2.0, 8.0 Hz, 1 H), 6.89 (d, J=8 Hz, 1 H), 3.79 (s, 2 H), 3.11-3.08 (m, 2 H), 2.82-2.79 (m, 2 H), 2.38 (brs, 1 H), 1.63-1.61 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871756B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-6a706332356f4b0e9bbff6491a3aebf3 |
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| Source note | uspto-grants-2014_10 |
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