Hydrochloric Acid → 3-Isobutylbenzaldehyde

HRID 249140ノート

反応式

HRID 249140 の反応式
[CH2:1]([C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[C:8]#N)[CH:2]([CH3:4])[CH3:3].[H-].C([Al+]CC(C)C)C(C)C.[Cl-].[NH4+].Cl.CC[O:28]CC>C1(C)C=CC=CC=1>[CH2:1]([C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH:8]=[O:28])[CH:2]([CH3:4])[CH3:3]

参加物

7

反応条件

温度
25 °C

実験手順

To a solution of 3-isobutylbenzonitrile (7.0 g) in toluene (150 ml) was added a 1.5M solution of diisobutylaluminum hydride in toluene (88 ml) at 25° C. over 30 minutes and the mixture was stirred at 25° C. for 2 hours. Another 1.5M solution of diisobutylaluminum hydride in toluene (30 ml) was added, and the mixture was stirred at 25° C. for 1 hour. The mixture was poured into a mixture of ether, aqueous ammonium chloride and 1N hydrochloric acid. The organic layer was separated, washed with water and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was chromatographed on silica gel (150 g) eluting with a mixture of toluene and hexane (2:1) to give 3-isobutylbenzaldehyde (4.72 g) as a colorless oil.

後処理

  1. stirringthe mixture was stirred at 25° C. for 1 hour
  2. customThe organic layer was separated
  3. washwashed with water and brine
  4. dry with materialdried over magnesium sulfate
  5. customAfter evaporation of the solvent
  6. customthe residue was chromatographed on silica gel (150 g)
  7. washeluting with a mixture of toluene and hexane (2:1)

出典と根拠

ORDレコード
ord-04a0a76c15b04bb6a1fa36254464ef4c
出典データセット
uspto-grants-1993_05
特許番号
US05212320

反応ノート

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