Nitric Acid → 4'-Nitrobiphenyl-4-yl benzoate
反応式
[C:1]([O:9][C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:12][CH:11]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N+:22]([O-])([OH:24])=[O:23]>C(O)(=O)C>[C:1]([O:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2[CH:21]=[CH:20][C:19]([N+:22]([O-:24])=[O:23])=[CH:18][CH:17]=2)=[CH:14][CH:15]=1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
反応条件
- 温度
- 85 °C
実験手順
A mixture of 274 g 4-benzoyloxybiphenyl (see Example 1) and 2000 ml glacial acetic acid is heated to 85° C. Then, 650 ml fuming nitric acid is dripped in such a manner that the temperature does not drop below 90° C. After cooling, the precipitate is filtered off, washed neutral with water and recrystallized from glacial acetic acid (melting point: 214° C.); yield: 60%.
後処理
- customdoes not drop below 90° C
- temperatureAfter cooling
- filtrationthe precipitate is filtered off
- washwashed neutral with water
- customrecrystallized from glacial acetic acid (melting point: 214° C.)
出典と根拠
- ORDレコード
- ord-0a32417a9d404269accc6e762f239e7a
- 出典データセット
- uspto-grants-1993_02
- 特許番号
- US05187237
反応ノート
読み込み中…