HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288805Generated: October 26, 2026
O-(o-Aminophenoxy)benzoic acid lactam → 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine
https://huagongshe.com/reaction/1288805
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-(o-Aminophenoxy)benzoic acid lactam | HCID 72374 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine | HCID 648933 | 96.1% |
Reaction Steps
In a dry 250 ml three-necked flask equipped with reflux condenser and thermometer, lithium aluminum hydride (1.8 g, 0.047 mol) was suspended in dry diethyl ether (75 ml) under a nitrogen atmosphere. Cautiously, 10,11-dihydrodibenz[b,f][1,4]oxazepin-11-one (5.0 g, 0.024 mol) was added in portions. The mixture was heated at reflux temperature for 5 hours, cooled to room temperature and left stirring overnight. The reaction mixture was quenched by cautious addition of water (1.8 ml), 4N sodium hydroxide (1.8 ml) and finally water (5.4 ml). Diethyl ether and toluene were added and the mixture was filtered. The filtercake was washed with diethyl ether, toluene and ethyl acetate, successively. The filtrate was evaporated until dryness, affording 4.55 g (96%) of 10,11-dihydrodibenz[b,f][1,4]oxazepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747481 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-daf18cbfc3d14a7993674d895d75af01 |
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| Source note | uspto-grants-1998_05 |
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