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    • 9. 发明授权
    • Process for nitrating aromatic amines
    • 硝化芳香胺的方法
    • US5922913A
    • 1999-07-13
    • US187949
    • 1998-11-06
    • Lowell J. LawrenceStefan KwiatkowskiPaul D. Smith
    • Lowell J. LawrenceStefan KwiatkowskiPaul D. Smith
    • C07C209/76C07C209/00
    • C07C209/76
    • Disclosed is a process of nitrating or dinitrating an aromatic amine compound that involves reacting the aromatic amine and nitric acid in the presence of acetic acid such that the molar ratio of the aromatic amine compound to acetic acid is from about 1:2 to about 1:16, and the molar ratio of nitric acid to the aromatic amine is between about 1.0 to about 1.5 times the nitric acid needed to complete the reaction. More particularly, the invention is a process of forming Pendimethalin, N-(1-ethylpropyl)-2,6-dinitro-3,4-xylidine, from N-(1-ethylpropyl)-3,4-xylidine (4-NAX) that involves reacting 4-NAX and nitric acid in the presence of acetic acid such that the molar ratio of nitric to the 4-NAX is between about 2:1 and about 3:1, preferably between about 2:1 and about 2.6:1, and such that the molar ratio of 4-NAX to acetic acid is between about 1:2 to about 1:16, preferably between about 1:4 and about 1:8.
    • 公开了一种芳族胺化合物的硝化或二硝化方法,其包括在乙酸存在下使芳族胺和硝酸反应,使得芳族胺化合物与乙酸的摩尔比为约1:2至约1:1。 16,硝酸与芳香胺的摩尔比为完成反应所需的硝酸的约1.0至约1.5倍。 更具体地说,本发明是由N-(1-乙基丙基)-3,4-二甲苯胺(4-NAX)形成二甲戊灵,N-(1-乙基丙基)-2,6-二硝基-3,4-二甲苯胺的方法 ),其包括在乙酸存在下使4-NAX和硝酸反应,使得硝酸与4-NAX的摩尔比为约2:1至约3:1,优选约2:1至约2.6:1。 1,使得4-NAX与乙酸的摩尔比为约1:2至约1:16,优选约1:4至约1:8。