Water → 2-(4-Nitro-1H-pyrazol-1-yl)ethan-1-ol
反応式
[N+:1]([C:4]1[CH:5]=[N:6][NH:7][CH:8]=1)([O-:3])=[O:2].[O:9]1[CH2:13][CH2:12]OC1=O.C(=O)([O-])[O-].[Cs+].[Cs+].O>CN(C)C=O.C(OCC)(=O)C>[N+:1]([C:4]1[CH:5]=[N:6][N:7]([CH2:12][CH2:13][OH:9])[CH:8]=1)([O-:3])=[O:2]参加物
7
反応条件
- 温度
- 100 °C
実験手順
A solid mixture of 4-nitro-1H-pyrazole (1 g, 8.84 mmol), 1,3-dioxolan-2-one (3.89 g, 44.2 mmol) and cesium carbonate (2.88 g, 8.84 mmol) was suspended in 20 ml dimethylformamide and the resulting suspension was slowly heated to 100° C. overnight. The mixture was added to 100 ml water and 40 ml ethyl acetate; the separated aqueous layer was extracted with ethyl acetate (30 ml), and the combined organic layers were washed with brine (30 ml), dried with magnesium sulfate, filtered and concentrated. The residue was flash chromatographed (50 mm; 2% methanol/methylene chloride then 4% methanol/methylene chloride) to give the title compound with some residual DMF.
後処理
- extractionthe separated aqueous layer was extracted with ethyl acetate (30 ml)
- washthe combined organic layers were washed with brine (30 ml)
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customchromatographed (50 mm
出典と根拠
- ORDレコード
- ord-a3b9a5837a2444289723ffe2c27776e4
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08426408B2
反応ノート
読み込み中…