Acetic Acid → 2-Hydrazinyl-4,6-dinitro-1,3-benzothiazole
反応式
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[C:7]([N+:14]([O-:16])=[O:15])[C:5]=2[N:6]=1.O.[NH2:18]N.O.C(O)(=O)C>C(OCCO)C>[NH:1]([C:2]1[S:3][C:4]2[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[C:7]([N+:14]([O-:16])=[O:15])[C:5]=2[N:6]=1)[NH2:18]参加物
6
実験手順
24.0 g of amino-4,6-dinitrobenzthiazole are heated to boiling for 1 hour in 200 ml of 2-ethoxyethanol with 20 ml of hydrazine hydrate (100% purity). After cooling to room temperature, the reaction mixture is poured into a mixture of 750 ml of water and 20 ml of glacial acetic acid, stirred for 1 hour, filtered off under suction, washed with water and dried. 21.0 g of 2-hydrazino-4,6-dinitrobenzthiazole are obtained. Melting point 210°-214° C. (decomposition). After recrystallization from 2-methoxyethanol. Melting point 216°-217° C. (decomposition).
後処理
- filtrationfiltered off under suction
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-05bfdc03b19248b5b83a449840a6eb88
- 出典データセット
- uspto-grants-1990_10
- 特許番号
- US04962040
反応ノート
読み込み中…