反応式
[C:1]([OH:18])(=[O:17])[C:2]1[C:3](=[CH:7][C:8](=[C:12]([CH:16]=1)[C:13]([OH:15])=[O:14])[C:9]([OH:11])=O)[C:4]([OH:6])=O>C1(OC)C=CC=CC=1>[CH:16]1[C:12]2[C:13]([O:14][C:9](=[O:11])[C:8]=2[CH:7]=[C:3]2[C:4]([O:18][C:1](=[O:17])[C:2]=12)=[O:6])=[O:15]参加物
3
試薬・触媒・溶媒 1
実験手順
50.0 g pyromellitic acid were boiled under reflux with 400 ml anisole and 3.0 g activated carbon, Merck Art. No. 2184, under the same conditions as in example 1 and then processed. 4.3 g (60.6% of the theory) water separated in the course of 2.5 hours. 27.3 g (=64% of the theory) pyromellitic acid anhydride were obtained and the remainder of 18.0 g, (36%) was filtered off as unchanged pyromellitic acid, together with the activated carbon.
後処理
- custom4.3 g (60.6% of the theory) water separated in the course of 2.5 hours
出典と根拠
- ORDレコード
- ord-56da8f3a68484008b231c5bed601bd04
- 出典データセット
- uspto-grants-1983_01
- 特許番号
- US04370487
関連ノート
読み込み中…