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    • 6. 发明公开
    • Method of producing 1,4-dihydroxy-2-naphthoic acid
    • Verfahren zur Herstellung von 1,4-Dihydroxy-2-Naphthalin-Carbonsaure。
    • EP0552019A2
    • 1993-07-21
    • EP93300190.1
    • 1993-01-13
    • SUMITOMO CHEMICAL COMPANY, LIMITEDSUMIKA FINE CHEMICALS Co., Ltd.
    • Nakamatsu, ToshioNishida, YasuhiroWatanabe, ShinichiKometani, Norio
    • C07C65/11C07C51/15
    • C07C51/15C07C65/11
    • A method of producing 1,4-dihydroxy-2-naphthoic acid comprises: subjecting 1,4-dihydroxynaphthalene to alkali metal salt formation reaction at a temperature of 110°C or more in an organic medium capable of dissolving 1,4-dihydroxynaphthalene, preferably selected from ketones, esters, monoalcohols, polyhydric alcohols and derivatives thereof and aromatic hydrocarbons using an alkali metal alcoholate, preferably of a Cl-4 alcohol; and subjecting the salt formation reaction mixture to carboxylation using carbon dioxide gas under atmospheric or increased pressure and preferably with an excess of CO₂ of 1.5 mols or more per mol of the dihydroxynaphthalene.
      The product is obtained easily and in a high yield, e.g of 80 to 92% and in high purity, and is useful as an intermediate for dyes, pigments and photographic agents.
    • 1,4-二羟基-2-萘甲酸的制造方法包括:在能够溶解1,4-二羟基萘的有机介质中,使1,4-二羟基萘在110℃以上的温度下进行碱金属盐形成反应, 优选选自酮,酯,一元醇,多元醇及其衍生物和使用碱金属醇盐,优选Cl-4醇的芳烃; 并且在大气压或增压下使用二氧化碳气体使盐形成反应混合物进行羧化,优选每摩尔二羟基萘过量的CO 2为1.5摩尔或更多。 该产品容易且以高产率例如80-92%和高纯度获得,并且可用作染料,颜料和照相剂的中间体。