Pyridine → 4-Acetoxy-2-(4-biphenylyl)-2-pentene
反応式
[C:1]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1C(=CC(O)C)C.[C:19]([O:22]C(=O)C)(=[O:21])[CH3:20].N1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[C:19]([O:22][CH:30]([CH3:31])[CH:29]=[C:28]([C:16]1[CH:15]=[CH:14][C:13]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)=[CH:18][CH:17]=1)[CH3:27])(=[O:21])[CH3:20]参加物
4
実験手順
To a solution of 0.9 g. of 2-(p-biphenylyl)-2-penten-4-ol (obtainable by Example 1) in 75 ml. of dry pyridine, 10 ml. of acetic anhydride is added. After 18 hours at room temperature, the mixture is poured onto ice and the solids filtered off and recrystallized from pentane to give 4-acetoxy-2-(4-biphenylyl)-2-pentene, m.p. 62°-64° C., which may also be designated 4-(p-biphenylyl)-penten-2-ol acetate.
後処理
- additionthe mixture is poured onto ice
- filtrationthe solids filtered off
- customrecrystallized from pentane
出典と根拠
- ORDレコード
- ord-afd2c3967717418abb6f7ad1ba354408
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04344966
反応ノート
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