Hydrochloric Acid → 1,3,5,7-Naphthalenetetracarboxylic acid
反応式
[C:1]1([C:20]([O-:22])=[O:21])[C:10]2[CH:9]=[C:8]([C:11]([O-:13])=[O:12])[CH:7]=[C:6]([C:14]([O-:16])=[O:15])[C:5]=2[CH:4]=[C:3]([C:17]([O-:19])=[O:18])[CH:2]=1.[K+].[K+].[K+].[K+].Cl>O>[C:1]1([C:20]([OH:22])=[O:21])[C:10]2[CH:9]=[C:8]([C:11]([OH:13])=[O:12])[CH:7]=[C:6]([C:14]([OH:16])=[O:15])[C:5]=2[CH:4]=[C:3]([C:17]([OH:19])=[O:18])[CH:2]=1参加物
4
実験手順
Crude tetrapotassium 1,3,5,7-naphthalenetetracarboxylate obtained in Example 13 was again dissolved in water, and the solution was acidified with hydrochloric acid to an acidity lower than pH 1 to form free crude 1,3,5,7-naphthalenetetracarboxylic acid. The product was separated and dried to form crude 1,3,5,7-naphthalenetetracarboxylic acid as shown in Table 7.
後処理
- customto form free crude 1,3,5,7-naphthalenetetracarboxylic acid
- customThe product was separated
- customdried
出典と根拠
- ORDレコード
- ord-4f61670b33994023acccadebe898a47f
- 出典データセット
- uspto-grants-1976_05
- 特許番号
- US03954840
反応ノート
読み込み中…