Methanol → HCID 20465144, compound

HRID 325553Notes

Reaction equation

HRID 325553 reaction equation
[H-].C([Al+]CC(C)C)C(C)C.[CH2:11]([NH:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][CH:22]=1)[C:18]#N)[CH:12]=[CH2:13].C[OH:24]>C1(C)C=CC=CC=1>[CH2:11]([NH:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][CH:22]=1)[CH:18]=[O:24])[CH:12]=[CH2:13]

Participants

5

Reactant 3

HCID 887MethanolHCID 15906009HCID 15906009, compoundHCID 21225700Diisobutylaluminumhydride

Product 1

HCID 20465144HCID 20465144, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Di-isobutylaluminum hydride (54 ml., 25% solution in toluene) is added with stirring to a solution of 12.1 g. of 3-(allylamino)benzonitrile under a nitrogen atmosphere. After addition is completed, the solution is stirred for one hour. A solution of methanol in toluene (50 ml., 1:1) is added over 30 minutes and the mixture is poured into 500 ml. vigorously stirred ice-cold 50% aqueous sulfuric acid. The mixture is filtered and the organic layer separated. The aqueous solution is extracted twice with toluene (100 ml.) and the combined organic layers are washed with aqueous sodium bicarbonate, dried over magnesium sulfate, decolorized with charcoal, filtered and evaporated in vacuo to give a light yellow crystalline solid. The product is recrystallized from dichloromethane/hexane giving colorless needles.

Workup

  1. additionAfter addition
  2. stirringthe solution is stirred for one hour
  3. additionthe mixture is poured into 500 ml
  4. filtrationThe mixture is filtered
  5. customthe organic layer separated
  6. extractionThe aqueous solution is extracted twice with toluene (100 ml.)
  7. washthe combined organic layers are washed with aqueous sodium bicarbonate
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. customevaporated in vacuo
  11. customto give a light yellow crystalline solid
  12. customThe product is recrystallized from dichloromethane/hexane giving colorless needles

Sources & evidence

ORD record
ord-904da358025d441aaa9b375e50ef5ff3
Source dataset
uspto-grants-1984_04
Patent number
US04440940

Reaction notes

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