Water → HCID 53719435, compound

HRID 1440981Notes

Reaction equation

HRID 1440981 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH:7]([C:10]1[C:15]([C:16](OCC)=[O:17])=[C:14]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:13]([C:27](OCC)=[O:28])=[C:12]([CH:32]([CH3:34])[CH3:33])[N:11]=1)([CH3:9])[CH3:8].O>CCOCC.O1CCCC1>[OH:17][CH2:16][C:15]1[C:10]([CH:7]([CH3:9])[CH3:8])=[N:11][C:12]([CH:32]([CH3:33])[CH3:34])=[C:13]([CH2:27][OH:28])[C:14]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1

Participants

6

Procedure

40.5 ml (40.5 mmol) of a 1 molar solution of lithium aluminum hydride in ether are added dropwise under nitrogen to a solution of 6.4 g (16.2 mmol) of the compound from Example 11 in 100 ml of dry tetrahydrofuran at 0° C. The mixture is stirred overnight at room temperature, warmed to 50° C. for 3 h and cooled again to 0° C. 200 ml of water are cautiously added dropwise to the mixture, and it is filtered over kieselgur with suction and washed with 250 ml of ether. The organic phase is separated, washed once with saturated sodium chloride solution, dried over magnesium sulphate and concentrated in vacuo. The residue is stirred with petroleum ether, and the precipitate is filtered off with suction and dried in a desiccator.

Workup

  1. temperaturewarmed to 50° C. for 3 h
  2. temperaturecooled again to 0° C
  3. filtrationis filtered over kieselgur with suction
  4. washwashed with 250 ml of ether
  5. customThe organic phase is separated
  6. washwashed once with saturated sodium chloride solution
  7. dry with materialdried over magnesium sulphate
  8. concentrationconcentrated in vacuo
  9. stirringThe residue is stirred with petroleum ether
  10. filtrationthe precipitate is filtered off with suction
  11. customdried in a desiccator

Sources & evidence

ORD record
ord-8d8ff6182c194df5b8b17b2154f6fa2f
Source dataset
uspto-grants-1996_03
Patent number
US05502057

Reaction notes

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