Aluminum isopropoxide → HCID 22464448, compound

HRID 236405Notes

Reaction equation

HRID 236405 reaction equation
CC(C)[O-].[Al+3].CC(C)[O-].CC(C)[O-].[O:14]=[C:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:17](=[O:24])[N:16]1[CH:25]([CH2:34][CH:35]([CH3:37])[CH3:36])[C:26]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=[O:27]>C(O)(C)C>[O:14]=[C:15]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:17](=[O:24])[N:16]1[CH:25]([CH2:34][CH:35]([CH3:37])[CH3:36])[CH:26]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[OH:27]

Participants

4

Procedure

Aluminum isopropoxide (125.6 g, 615 mmcl) was added to a suspension of 2-(1,3-dioxo-2-azaindane-2-yl)-4-methyl-1-phenylpentane-1-one (72.3 g, 225 mmcl) in isopropanol (1,000 ml). The mixture was heated under reflux for 6.5 hours. The isopropanol was removed by distillation under reduced pressure and the residue was added with ethyl acetate (800 ml) and further with an aqueous solution of sodium sulfate. The resulting organic layer was decanted and the residue was washed twice with ethyl acetate (200 ml). The combined organic layer was washed with brine. The organic solution was dried and the solvent was removed by distillation under reduced pressure. The residue was recrystallized twice from benzene to obtain 29.3 g of the intended compound as white crystals (yield: 40%).

Workup

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 6.5 hours
  3. customThe isopropanol was removed by distillation under reduced pressure
  4. additionthe residue was added with ethyl acetate (800 ml) and further with an aqueous solution of sodium sulfate
  5. customThe resulting organic layer was decanted
  6. washthe residue was washed twice with ethyl acetate (200 ml)
  7. washThe combined organic layer was washed with brine
  8. customThe organic solution was dried
  9. customthe solvent was removed by distillation under reduced pressure
  10. customThe residue was recrystallized twice from benzene

Sources & evidence

ORD record
ord-88bfc3f4f2424bfa866eefae01caadb3
Source dataset
uspto-grants-1987_02
Patent number
US04644063

Reaction notes

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