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1-Amino-anthraquinone-2-carboxylic acid cpds. prodn. from 2-methyl cpds. - by oxidn. with nitrobenzene in aq. inorganic base using phase transfer catalyst
1-Amino-anthraquinone-2-carboxylic acid cpds. prodn. from 2-methyl cpds. - by oxidn. with nitrobenzene in aq. inorganic base using phase transfer catalyst
Prodn. of 1-aminoanthraquinone-2-carboxylic acids of formula (I) by oxidn. of 1-amino-2-methylanthraquinones of formula (II); X = H, Cl or Br; with nitrobenzene (III) under alkaline conditions, followed by acidification of the reaction mixt., the novelty is that oxidn. is carried out in an aq. inorganic base (IV) in the presence of a phase transfer catalyst. Pref. (IV) is an aq. soln. or suspension or alkali(ne earth) hydroxide, eps. NaOH. Oxidn. is carried out at 90-140 deg.C. USE/ADVANTAGE - (I) are used in dyestuff synthesis. They are obtd. in good yield and good purity, suitable for direct use for this purpose, by a simple and economical process, which is suitable for continuous or batch operatio
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机译:产品式(I)的1-氨基蒽醌-2-羧酸的氧化反应式(II)的1-氨基-2-甲基蒽醌; X = H,Cl或Br;在碱性条件下用硝基苯(III)进行酸化,然后酸化反应混合物,新颖之处在于氧化。在水溶液中进行。相转移催化剂存在下的无机碱(IV)。首选(IV)是水溶液soln。或悬浮液或碱(碱土)氢氧化物,eps。氢氧化钠氧化。在90-140℃下进行。用途/优点-(I)用于染料合成。他们很肥胖。具有高收率和高纯度的特点,适合通过简单,经济的方法直接用于此目的,适合连续或间歇操作
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