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Imidazole → 1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzene

HRID 341367
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HRID 341367 반응식
[I:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[Si:9](Cl)([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10].N1C=CN=C1>ClCCl>[C:12]([Si:9]([O:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1)([CH3:11])[CH3:10])([CH3:15])([CH3:14])[CH3:13]
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참가 물질

5

반응물 3

HCID 795ImidazoleHCID 108944-IodophenolHCID 28928tert-Butyldimethylsilyl chloride

생성물 1

HCID 148035271-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzene수율 95.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-Iodophenol (1.0 g, 4.55 mmol) was dissolved in dichloromethane (5 mL). tert-Butyldimethylsilyl chloride (0.685 g, 4.55 mmol) and imidazole (0.309 g, 4.55 mmol) were added. The reaction was stirred overnight at room temperature. The reaction mixture was partitioned between water (30 mL) and dichloromethane (30 mL). The organic layer was removed and the aqueous layer was extracted with dichloromethane (30 mL). The organic layers were combined, dried and concentrated, and the residue was purified by chromatography (0-10% EtOAc/hexanes) to give the title compound as a light yellow oil (1.45 g, 94%).

후처리

  1. customThe reaction mixture was partitioned between water (30 mL) and dichloromethane (30 mL)
  2. customThe organic layer was removed
  3. extractionthe aqueous layer was extracted with dichloromethane (30 mL)
  4. customdried
  5. concentrationconcentrated
  6. customthe residue was purified by chromatography (0-10% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-c267bed69794477a91684b8b46a69e9d
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895776B2

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