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Imidazole → 2-((Tert-butyldimethylsilyloxy)methyl)thiazole

HRID 244483
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HRID 244483 반응식
[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH2:6][OH:7].N1C=CN=C1.[Si:13](Cl)([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]>C(Cl)Cl>[Si:13]([O:7][CH2:6][C:2]1[S:1][CH:5]=[CH:4][N:3]=1)([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 27952131,3-Thiazol-2-ylmethanol

생성물 1

HCID 214805922-((Tert-butyldimethylsilyloxy)methyl)thiazole수율 100.9%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a room temperature solution of thiazol-2-ylmethanol (1.00 g, 8.684 mmol) in CH2Cl2 was added imidazole (1.18 g, 17.4 mmol) followed by tert-butyldimethylsilyl chloride (1.70 g, 11.3 mmol). After 30 minutes, the mixture was quenched with 2 mL of MeOH and passed through a pad of silica gel eluting with CH2Cl2 (700 mL) and concentrated in vacuo to afford 2.01 g (100%) of the title compound.

후처리

  1. customthe mixture was quenched with 2 mL of MeOH
  2. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-88ca08a0697a4cb59eae2472cba07378
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658637B2

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