反応式
[OH:1][CH2:2][C:3]([CH2:9][OH:10])([CH2:7][OH:8])[N+:4]([O-:6])=[O:5].CO[C:13](OC)([CH3:15])[CH3:14]>Cl.C(#N)C>[CH3:14][C:13]1([CH3:15])[O:8][CH2:7][C:3]([CH2:9][OH:10])([N+:4]([O-:6])=[O:5])[CH2:2][O:1]1参加物
5
反応条件
- 温度
- 80 °C
実験手順
To a 250 ml round bottom flask equipped with a stir bar was added 5 g (0.03 mol) tris(hydroxymethyl) nitromethane, 3.75 g (0.36 mol) 2,2-dimethoxypropane, 100 ml acetonitrile and 6 drops concentrated hydrochloric acid. The reaction was heated to 80° C. for 18 hours. After cooling to room temperature tte volatiles were removed in vacuo to give a white solid 2,2-dimethyl-5-hydroxy methyl-5-nitro-1,3-dioxane in 82% yield.
後処理
- customTo a 250 ml round bottom flask equipped with a stir bar
- temperatureAfter cooling to room temperature tte volatiles
- customwere removed in vacuo
出典と根拠
- ORDレコード
- ord-4cb4e03e4c7a4972819b706c2c63d137
- 出典データセット
- uspto-grants-1990_12
- 特許番号
- US04978793
関連ノート
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