O-(o-Aminophenoxy)benzoic acid lactam → 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine

HRID 1956474Notes

Reaction equation

HRID 1956474 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]=1

Participants

4

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

  1. customIn a dry 250 ml three-necked flask equipped
  2. temperaturewith reflux condenser
  3. temperatureThe mixture was heated
  4. temperatureat reflux temperature for 5 hours
  5. waitleft
  6. 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)
  7. additionDiethyl ether and toluene were added
  8. filtrationthe mixture was filtered
  9. washThe filtercake was washed with diethyl ether, toluene and ethyl acetate
  10. customThe filtrate was evaporated until dryness

Sources & evidence

ORD record
ord-6f4b0dfd67644b34892b0b18c9bffb62
Source dataset
uspto-grants-1998_07
Patent number
US05780486

Reaction notes

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