HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235169Generated: October 31, 2026
Methanol → 8-Bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine
https://huagongshe.com/reaction/2235169
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | 7-Bromo-1,2,3,4-tetrahydronaphthalen-1-one | HCID 252731 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 8-bromo-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one | HCID 5092620 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine | HCID 16244474 | 92% |
Reaction Steps
Borane tetrahydrofuran complex (1 M solution in tetrahydrofuran, 21 mL, 21 mmol) was added to a solution of 8-bromo-1,3,4,5-tetrahydro-benzo[b]azepin-2-one (prepared from 7-bromo-3,4-dihydro-2H-naphthalen-1-one in analogy with the general procedure described in J Chem. Soc. (C) 1969, 183; 1.00 g, 4.17 mmol) in tetrahydrofuran, and the solution was heated at reflux for 2 h. After cooling, methanol (21 mL) was added, and volatile material was removed by distillation. The residue was taken up in 5% ethanolic sulfuric acid solution (12 mL) and heated at reflux for 2 h, then basified to pH 10 by addition of 2 M aq. sodium hydroxide solution and partitioned between water and ethyl acetate. The organic layer was dried (MgSO4) and evaporated. Chromatography (SiO2, heptane-ethyl acetate 2:1) yielded 8-bromo-2,3,4,5-tetrahydro-1H-benzo[b]azepine (865 mg, 92%). White solid, MS (ISP) m/e 226.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713996B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-d7aa74c309c543318abeb17a23688049 |
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| Source note | uspto-grants-2010_05 |
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