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Imidazole → N-cyclopentyl-O-tert-butyldimethylsilylhydroxylamine

HRID 895153
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HRID 895153 반응식
N1C=CN=[CH:2]1.[C:6]([SiH:10](Cl)[CH3:11])([CH3:9])([CH3:8])[CH3:7].[CH:13]1([NH:18][OH:19])[CH2:17][CH2:16][CH2:15][CH2:14]1>CN(C)C=O.C(OCC)(=O)C.CCCCCC>[CH:13]1([NH:18][O:19][Si:10]([C:6]([CH3:9])([CH3:8])[CH3:7])([CH3:11])[CH3:2])[CH2:17][CH2:16][CH2:15][CH2:14]1
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참가 물질

7

반응물 3

HCID 795ImidazoleHCID 10219393N-cyclopentylhydroxylamineHCID 102463549Tert-butylmethylsilyl chloride

생성물 1

HCID 22385752N-cyclopentyl-O-tert-butyldimethylsilylhydroxylamine수율 52.1%

시약·촉매·용매 3

HCID 6228Dimethylformamide용매HCID 8058Hexane
용매
HCID 8857Ethyl Acetate용매

실험 절차

Imidazole (882 mg) and tert-butylmethylsilyl chloride (903 mg) were added to N-cyclopentylhydroxylamine (650 mg, 6.43 mmol) in dimethylformamide (10 ml). The mixture was stirred at room temperature for 3 hours. After diluting the mixture with ethyl acetate and hexane, the organic layer was washed with water and saturated aqueous sodium chloride. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (hexane-ethyl acetate, 20:1 to 10:1) to give the title compound (722 mg) as a colorless oil.

후처리

  1. washthe organic layer was washed with water and saturated aqueous sodium chloride
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by silica gel chromatography (hexane-ethyl acetate, 20:1 to 10:1)

출처 및 근거

ORD 기록
ord-84347f0dee2743adbbf6297953be81fb
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06914062B2

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