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Imidazole → 1-((2-(Trimethylsilyl)ethoxy)methyl)-1H-imidazole

HRID 500796
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HRID 500796 반응식
[H-].[Na+].[NH:3]1[CH:7]=[CH:6][N:5]=[CH:4]1.Cl[CH2:9][O:10][CH2:11][CH2:12][Si:13]([CH3:16])([CH3:15])[CH3:14].CO.CCOC(C)=O>C1COCC1>[CH3:14][Si:13]([CH3:16])([CH3:15])[CH2:12][CH2:11][O:10][CH2:9][N:3]1[CH:7]=[CH:6][N:5]=[CH:4]1
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참가 물질

6

반응물 4

HCID 795ImidazoleHCID 24758Sodium hydrideHCID 27242712-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 21584119Ethylacetate methanol

생성물 1

HCID 110526051-((2-(Trimethylsilyl)ethoxy)methyl)-1H-imidazole수율 70%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

To a stirred suspension of NaH (60% dispersion in oil, 0.65 g, 16.2 mmol) at 0° C. was added imidazole (1 g, 14.7 mmol) in THF (14 mL). The mixture was warmed to room temperature over 30 min, then re-cooled to 0° C. followed by an addition of (2-(chloromethoxy)ethyl)trimethylsilane (2.73 ml, 15.4 mmol). The combined mixture was warmed to room temperature over 1 h, quenched with saturated aqueous ammonium chloride, concentrated to dryness and partitioned between water and EtOAc. Organic phase was collected, dried over anhydrous sodium sulfate, filtered and evaporated. The residue was purified by column chromatography (eluents EtOAc, then MeOH/EtOAc 20:80), to afford the title compound (2.04 g, 70% yield) as a white solid. MS (m/z) 199.3 (M+H).

후처리

  1. temperaturere-cooled to 0° C.
  2. temperatureThe combined mixture was warmed to room temperature over 1 h
  3. customquenched with saturated aqueous ammonium chloride
  4. concentrationconcentrated to dryness
  5. custompartitioned between water and EtOAc
  6. customOrganic phase was collected
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue was purified by column chromatography (eluents EtOAc

출처 및 근거

ORD 기록
ord-c09c286d156c44bdb3b4d7d1453c64da
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07772247B2

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