HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718090Generated: October 26, 2026
Ethanol → 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine
https://huagongshe.com/reaction/718090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | O-(o-Aminophenoxy)benzoic acid lactam | HCID 72374 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine | HCID 648933 | 101.9% |
Reaction Steps
Dibenzo[b,f][1,4]oxazepin-11(10H)-one (1.001 g, 4.7 mmol) was dissolved in THF (20 mL) and the borane (2M in THF, 20 mL, 40.0 mmol) was added. The reaction mixture was refluxed for 3 hours. The mixture was cooled down to room temperature and an excess of ethanol was added to quench the reaction. The resulting mixture was refluxed for 2 hours. The mixture was cooled down and concentrated in vacuo. The residue was dissolved in ethyl acetate and the organic layer was washed with water and brine, dried over sodium sulfate, filtered and evaporated to afford title compound 398 (0.945 g, quantitative). MS (m/z): 198.1 (M+H). 1H NMR (CD3OD) δ (ppm): 7.29-7.19 (m, 2H), 7.16-7.04 (m, 2H), 7.01-6.99 (m, 1H), 6.82-6.78 (m, 1H), 6.63-6.59 (m, 2H), 4.88 (s, 1H), 4.39 (s, 2H). MS (m/z): 198.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193749B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-6c872bd1a2d4474e95de9b5e2627a6bc |
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| Source note | uspto-grants-2015_11 |
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