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Imidazole → N-cyclopentyl-O-tert-butyldimethylsilylhydroxylamine

HRID 857867
ノート
印刷プレビュー

反応式

HRID 857867 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

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

生成物 1

HCID 22385752N-cyclopentyl-O-tert-butyldimethylsilylhydroxylamine収率 52.1%

試薬・触媒・溶媒 3

HCID 6228Dimethylformamide溶媒HCID 8058Hexane
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-7edb67e9f7664ac4a3c3bfbb906994af
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07148224B2

反応ノート

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