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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(o-Aminophenoxy)benzoic acid lactamHCID 72374—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product10,11-Dihydrodibenzo(b,f)(1,4)oxazepineHCID 64893396.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747481
Source datasetuspto-grants-1998_05
ORD IDord-daf18cbfc3d14a7993674d895d75af01
Source noteuspto-grants-1998_05