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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBoraneHCID 6331—
ReactantO-(o-Aminophenoxy)benzoic acid lactamHCID 72374—
SolventTetrahydrofuranHCID 8028—
Product10,11-Dihydrodibenzo(b,f)(1,4)oxazepineHCID 648933101.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193749B2
Source datasetuspto-grants-2015_11
ORD IDord-6c872bd1a2d4474e95de9b5e2627a6bc
Source noteuspto-grants-2015_11