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Diethyl Ether → 4-(p-Chlorophenyl)-4-methyl-2-pentenal

HRID 610849
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인쇄 미리보기

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HRID 610849 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:15])([CH3:14])[C:9](F)=[CH:10][C:11]#N)=[CH:4][CH:3]=1.[H-].C([Al+]CC(C)C)C(C)C.C([O:28]CC)C>CCCCCC.O.Cl>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:15])([CH3:14])[CH:9]=[CH:10][CH:11]=[O:28])=[CH:4][CH:3]=1
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참가 물질

7

반응물 3

HCID 3283Diethyl EtherHCID 21225700DiisobutylaluminumhydrideHCID 542690284-(p-Chlorophenyl)-3-fluoro-4-methyl-2-pentenenitrile

생성물 1

HCID 539399194-(p-Chlorophenyl)-4-methyl-2-pentenal수율 97%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 962
Water
용매
HCID 8058Hexane용매

반응 조건

온도
-40 °C

실험 절차

A solution of 4-(p-chlorophenyl)-3-fluoro-4-methyl-2-pentenenitrile, (Z)- (15.6 g, 69.7 mmol) in diethyl ether is treated dropwise with diisobutylaluminum hydride (83.6 mmol, 83.6 mL of a 1M solution in hexane) over 90 minutes at -45° C. under nitrogen, stirred at -40° C. for 35 minutes, and diluted sequentially with water and 2N hydrochloric acid at -10° C. The resultant aqueous mixture is stirred at room temperature for one hour and extracted with diethyl ether. The organic extracts are combined, washed sequentially with water, 2N hydrochloric acid and water, dried over anhydrous sodium sulfate, and concentrated in vacuo to give the title product as a brown oil (15.34 g, 97% yield).

후처리

  1. stirringThe resultant aqueous mixture is stirred at room temperature for one hour
  2. extractionextracted with diethyl ether
  3. washwashed sequentially with water, 2N hydrochloric acid and water
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f6e435d6224c4651ad1c500264928ec7
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05998673

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