Water → 2-(1-Methylethyl)-5,9-dimethyl-2,4,8-decatrienal

HRID 1707781

반응식

HRID 1707781 반응식
[CH3:1][CH:2]([C:4](=[CH:7][CH:8]=[C:9]([CH3:16])[CH2:10][CH2:11][CH:12]=[C:13]([CH3:15])[CH3:14])[C:5]#N)[CH3:3].[H-].C([Al+]CC(C)C)C(C)C.[OH2:27]>CCCCCC.C1(C)C=CC=CC=1>[CH3:1][CH:2]([C:4](=[CH:7][CH:8]=[C:9]([CH3:16])[CH2:10][CH2:11][CH:12]=[C:13]([CH3:15])[CH3:14])[CH:5]=[O:27])[CH3:3]

참가 물질

6

반응 조건

온도
-70 °C

실험 절차

To a solution of 2-(1-methylethyl)-5,9-dimethyl-2,4,8-decatrienenitril (2Z compound, 217 mg, 1 mmol) in n-hexane (4 ml) was added a 1 M solution of diisobutylaluminium hydride in toluene (2 ml) with stirring under argon atmosphere at -70° C. After two-hour-stirring at the same temperature, water (0.8 ml) was added to the mixture followed by removal of the cooling bath and vigorous stirring. The resultant while precipitates were filtered and washed with n-hexane. The filtrate was combined with a 10% aqueous solution of oxalic acid and stirred for 3 hours. The organic layer was extracted and separated, washed with water, dried over MgSO4, and concentrated. The above manipulation was conducted under argon atmosphere. The resultant residue was subjected to silica gel column chromatography (solvent: n-hexane/ethyl acetate=50:l) to obtain the aimed 2-(1-methylethyl)-5,9-dimethyl-2,4,8-decatrienal (198 mg, 90%).

후처리

  1. additionwas added to the mixture
  2. customfollowed by removal of the cooling bath and vigorous stirring
  3. customThe resultant while precipitates
  4. filtrationwere filtered
  5. washwashed with n-hexane
  6. stirringstirred for 3 hours
  7. extractionThe organic layer was extracted
  8. customseparated
  9. washwashed with water
  10. dry with materialdried over MgSO4
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3391ceb1238740f986eb395fe1b3bce3
출처 데이터셋
uspto-grants-1994_10
특허 번호
US05354874

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