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Imidazole → 1-(1H-imidazol-1-yl)-3-methyl-2-butanol

HRID 496434
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HRID 496434 반응식
[CH:1]([CH:4]1[CH2:6][O:5]1)([CH3:3])[CH3:2].[NH:7]1[CH:11]=[CH:10][N:9]=[CH:8]1>C(#N)C>[N:7]1([CH2:6][CH:4]([OH:5])[CH:1]([CH3:3])[CH3:2])[CH:11]=[CH:10][N:9]=[CH:8]1
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참가 물질

4

반응물 2

HCID 795ImidazoleHCID 1026181,2-Epoxy-3-methylbutane

생성물 1

HCID 223247001-(1H-imidazol-1-yl)-3-methyl-2-butanol수율 46%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A solution of 2-isopropyloxirane (2.28 g, 26 mmol) and imidazole (1.80 g, 26 mmol) in acetonitrile (25 mL) was stirred at reflux for 16 h. The mixture was concentrated, and the residue was purified by flash column chromatography (SiO2, CH2Cl2-methanol-ammonium hydroxide 80:20:1) to give 1-(1H-imidazol-1-yl)-3-methyl-2-butanol as a yellow oil, 1.88 g, 46% yield. NMR spectrum was consistent with structure. MS EI: M+• 154.1103 (M+• −154.1106). 4. 6-hydroxy-5-[(phenylsulfonyl)methyl]-3,4-dihydro-1(2H)-naphthalenone

후처리

  1. temperatureat reflux for 16 h
  2. concentrationThe mixture was concentrated
  3. customthe residue was purified by flash column chromatography (SiO2, CH2Cl2-methanol-ammonium hydroxide 80:20:1)

출처 및 근거

ORD 기록
ord-a76fd5db663444ac9ce001ed4653921c
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06943183B2

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