2-(3-nitro-1H-pyrazol-1-yl)ethanol → 2-(3-Amino-1H-pyrazol-1-yl)ethan-1-ol
反応式
[N+:1]([C:4]1[CH:8]=[CH:7][N:6]([CH2:9][CH2:10][OH:11])[N:5]=1)([O-])=O.[H][H]>C(O)C.[Pd]>[NH2:1][C:4]1[CH:8]=[CH:7][N:6]([CH2:9][CH2:10][OH:11])[N:5]=1参加物
5
実験手順
A solution 2-(3-nitro-pyrazol-1-yl)-ethanol (3.46 g, 22.02 mmol) in ethanol (40 mL) was placed in a Parr shaker bottle and treated with 10% palladium on carbon (350 mg). The bottle was then put on the Parr shaker and charged with hydrogen to 50 psi and let shake for 1 h. After this time, the reaction mixture was filtered through celite and the celite washed with ethanol. The filtrate was then concentrated in vacuo and azeotroped with acetonitrile and then chloroform to afford 2-(3-amino-pyrazol-1-yl)-ethanol (3.02 g, >quant.) as a light yellow viscous oil: 1H NMR (300 MHz, DMSO-d6 δ ppm 7.26 (d, J=1.83 Hz, 1H), 5.34 (d, J=2.20 Hz, 1H), 4.76 (t, J=5.31 Hz, 1H), 4.50 (s, 2H), 3.78-3.88 (m, 2H), 3.62 (q, J=5.74 Hz, 2H).
後処理
- filtrationAfter this time, the reaction mixture was filtered through celite
- washthe celite washed with ethanol
- concentrationThe filtrate was then concentrated in vacuo
- customazeotroped with acetonitrile
出典と根拠
- ORDレコード
- ord-2459a1673ec34672b976dd713410ab5d
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08470866B2
反応ノート
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