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Diethyl Ether → 4-Phenylbutanal

HRID 986064
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HRID 986064 반응식
[C:1]1([CH2:7][CH2:8][CH2:9][C:10]#N)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].C([Al+]CC(C)C)C(C)C.CC[O:24]CC>C1(C)C=CC=CC=1>[C:1]1([CH2:7][CH2:8][CH2:9][CH:10]=[O:24])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 74897BenzenebutanenitrileHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 290304-Phenylbutanal

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a stirred suspension of 4-phenylbutyronitrile (21.7 g, 0.12 mole) in ether (400 ml) at 78° C. is added 85 ml. of 25.3% diisobutylaluminum hydride in toluene over a period of 1 hour. After an additional 1 hour, the dry ice-acetone bath is removed and the reaction mixture is stirred at ambient temperature for 3 hours. The reaction mixture is added slowly to 5% aqueous sulfuric acid and then is extracted with several portions of ether. The ether extracts are combined, washed with water and saturated aqueous sodium chloride solution and dried over magnesium sulfate. After removal of the ether, the residual yellow oil is distilled in vacuo to give an oil.

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후처리

  1. additionis added 85 ml
  2. customthe dry ice-acetone bath is removed
  3. additionThe reaction mixture is added slowly to 5% aqueous sulfuric acid
  4. extractionis extracted with several portions of ether
  5. washwashed with water and saturated aqueous sodium chloride solution
  6. dry with materialdried over magnesium sulfate
  7. customAfter removal of the ether
  8. distillationthe residual yellow oil is distilled in vacuo
  9. customto give an oil

출처 및 근거

ORD 기록
ord-d02d0d3735ad4cc7a2340ea5d1bd5551
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04710513

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