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Pyridine → HCID 19010792, 화합물

HRID 1741832
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HRID 1741832 반응식
N1C=CC=CC=1.[CH2:7]([C:11]1[CH:16]=[CH:15][C:14]([CH:17]([OH:21])[CH2:18][CH:19]=[CH2:20])=[CH:13][CH:12]=1)[CH:8]([CH3:10])[CH3:9]>ClCCl.[O-2].[Cr+6].[O-2].[O-2]>[CH2:7]([C:11]1[CH:12]=[CH:13][C:14]([C:17](=[O:21])[CH2:18][CH:19]=[CH2:20])=[CH:15][CH:16]=1)[CH:8]([CH3:10])[CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 1049PyridineHCID 190107494-(2-Methylpropyl)-α-2-propen-1-ylbenzenemethanol

생성물 1

HCID 19010792HCID 19010792, 화합물수율 81.6%

시약·촉매·용매 2

HCID 10219390chromium (VI) trioxide촉매HCID 6344Dichloromethane용매2회

실험 절차

To a stirred solution of pyridine (1.98 ml) in dichloromethane (15 ml) was added chromium(VI) oxide (1.23 g) at 0° C. After 30 minutes, 1-(4-isobutylphenyl)-3-buten-1-ol (525 mg) in dichloromethane (2 ml) was added and stirred for 20 minutes at ambient temperature. The reaction mixture was filtered through Florisil and washed with ether. The filtrate was concentrated in vacuo and chromatographed on silica gel (hexane:dichloromethane=1:1) to give 1-(4-isobutylphenyl)-3-buten-1-one (424 mg).

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후처리

  1. filtrationThe reaction mixture was filtered through Florisil
  2. washwashed with ether
  3. concentrationThe filtrate was concentrated in vacuo
  4. customchromatographed on silica gel (hexane:dichloromethane=1:1)

출처 및 근거

ORD 기록
ord-d7daae02ffee47a89fb280c653ca915a
출처 데이터셋
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05334716

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