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5-(4-Methoxyphenyl)pent-4-yn-1-ol → 5-(4-Methoxyphenyl)pentane-1-ol

HRID 25101
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인쇄 미리보기

반응식

HRID 25101 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]#[C:10][CH2:11][CH2:12][CH2:13][OH:14])=[CH:5][CH:4]=1.[H][H]>[Pd].C(O)C>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][OH:14])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 115501385-(4-Methoxyphenyl)pent-4-yn-1-olHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 128629555-(4-Methoxyphenyl)pentane-1-ol수율 93.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매2회

실험 절차

A solution of 16 (7.1 g, 37 mmol) in 150 dry ethanol (150 mL) was placed in a 0.5 L Parr flask and palladium on carbon (0.92 g, 5% wet. Pd/C) was added as a suspension in ethanol (25 mL). The reaction mixture was shaken at 50 psi of hydrogen pressure at room temperature for 24 hours. After this time, the mixture was filtered through a silica gel pad and the solvent was removed at reduced pressure. The residue was purified by flash chromatography (silica gel, 1:3 ethyl acetate/hexanes) to provide 17 (6.7 g, 92%) as a clear oil. 1H NMR (300 MHz, CDCl3) δ1.48 (m, 2H), 1.60 (m, 4H), 2.58 (m, 2H), 3.63 (m, 2H) 3.80 (s, 3H), 6.83 (d, 2H), 7.10 (d, 2H).

후처리

  1. filtrationAfter this time, the mixture was filtered through a silica gel pad
  2. customthe solvent was removed at reduced pressure
  3. customThe residue was purified by flash chromatography (silica gel, 1:3 ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-114306deb5744f5a827d9dfe52c8a547
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06858614B2

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