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Aluminium lithium hydride → 3-(4'-Cyclopentylphenyl)-2-butenol

HRID 1582679
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HRID 1582679 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH:7]1([C:12]2[CH:17]=[CH:16][C:15]([C:18]([CH3:25])=[CH:19][C:20](OCC)=[O:21])=[CH:14][CH:13]=2)[CH2:11][CH2:10][CH2:9][CH2:8]1>CCOCC>[CH:7]1([C:12]2[CH:13]=[CH:14][C:15]([C:18]([CH3:25])=[CH:19][CH2:20][OH:21])=[CH:16][CH:17]=2)[CH2:8][CH2:9][CH2:10][CH2:11]1
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참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 69907173Ethyl 3-(4-cyclopentylphenyl)but-2-enoate

생성물 1

HCID 699071583-(4'-Cyclopentylphenyl)-2-butenol수율 82.3%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

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온도
0 °C

실험 절차

To an ice cooled slurry of LiAlH4 (2.7 g) in dry ether (150 ml) was added a solution of ethyl 3-(4′-cyclopentylphenyl)-but-2-enoate (3a, 8.2 g) in dry ether (50 ml) dropwise. The mixture was stirred at 0° C. for 3 h. The reaction mixture was quenched with water (10 ml). A solution of 10% NaOH (5 ml) was added and then ether layer was decanted. The precipitate was washed with ether and combined organic layer was concentrated. The crude product was purified by column chromatography on silica gel to give 5.6 g (82.3% yield) of 3-(4′-cyclopentylphenyl)-2-butenol (4a, formula 4, R=cyclopentyl) as oil.

후처리

  1. customThe reaction mixture was quenched with water (10 ml)
  2. additionA solution of 10% NaOH (5 ml) was added
  3. customether layer was decanted
  4. washThe precipitate was washed with ether and combined organic layer
  5. concentrationwas concentrated
  6. customThe crude product was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-461d66409cb14efc86e72017e20951c7
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06737438B2

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