O-(o-Aminophenoxy)benzoic acid lactam → 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH:7]1[C:12]2[C:13](=O)[NH:14][C:15]3[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=3[O:17][C:11]=2[CH:10]=[CH:9][CH:8]=1>C(OCC)C>[CH:7]1[C:12]2[CH2:13][NH:14][C:15]3[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=3[O:17][C:11]=2[CH:10]=[CH:9][CH:8]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
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.
Workup
- customIn a dry 250 ml three-necked flask equipped
- temperaturewith reflux condenser
- temperatureThe mixture was heated
- temperatureat reflux temperature for 5 hours
- waitleft
- customThe reaction mixture was quenched by cautious addition of water (1.8 ml), 4N sodium hydroxide (1.8 ml) and finally water (5.4 ml)
- additionDiethyl ether and toluene were added
- filtrationthe mixture was filtered
- washThe filtercake was washed with diethyl ether, toluene and ethyl acetate
- customThe filtrate was evaporated until dryness
Sources & evidence
- ORD record
- ord-daf18cbfc3d14a7993674d895d75af01
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05747481
Reaction notes
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