反応式
[N+:1]([C:4]1[CH:9]=[C:8]([NH2:10])[CH:7]=[CH:6][C:5]=1[NH2:11])([O-:3])=[O:2].O1CCOCC1.C(OCC)C.[ClH:23]>C(O)C>[ClH:23].[N+:1]([C:4]1[CH:9]=[C:8]([NH2:10])[CH:7]=[CH:6][C:5]=1[NH2:11])([O-:3])=[O:2]参加物
6
実験手順
A solution comprising 2-nitro-1,4-phenylenediamine (21.0 g, 137 mmol) in ethanol (350 mL) and 4.0M hydrogen chloride in dioxane (30.8 mL, 123 mmol) was stirred at room temperature for 15 minutes and then diethyl ether (1 L) was added to give a precipitate. The precipitate was collected by filtration, washed with additional diethyl ether and dried in vacuo to provide 2-nitro-1,4-phenylenediamine hydrochloride (23.3 g, 100% yield).
後処理
- customto give a precipitate
- filtrationThe precipitate was collected by filtration
- washwashed with additional diethyl ether
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-1c90099f0e974701bfe7210ffb4a525c
- 出典データセット
- uspto-grants-2003_05
- 特許番号
- US06562854B2
関連ノート
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