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    • 3. 发明授权
    • Process for producing 2,6-dihydroxy-3,4-dialkylpyridines
    • 2,6-二羟基-3,4-二烷基吡啶的制备方法
    • US06624307B1
    • 2003-09-23
    • US10109434
    • 2002-03-28
    • Murugappa VedachalamJon Kirk Smith
    • Murugappa VedachalamJon Kirk Smith
    • C07D21309
    • C07D213/69
    • Commercially viable process for producing 2,6-dihydroxy-3,4-dimethlpridine. The process includes reacting 2-cyanoacetamide with sodium methoxide followed by condensation with ethyl 2-methylacetoacetate in methanol to give the sodium salt of 2,6-dihydroxy-4,5-dimethyl-3-pyridinecarbonitrile. The sodium salt of 2,6-dihydroxy-4,5-dimethyl-3-pyridinecarbonitrile is hydrolyzed with hydrobromic acid and decarboxylated to the hydrobromide salt of 2,6-dihydroxy-3,4-dimethylpyridine. The desired 2,6-dihydroxy-3,4-dimethylpyridine is produced from the hydrobromide salt by neutralizing the same with sodium hydroxide.
    • 用于生产2,6-二羟基-3,4-二甲基吡啶的商业上可行的方法。 该方法包括使2-氰基乙酰胺与甲醇钠反应,然后与2-甲基乙酰乙酸乙酯在甲醇中缩合,得到2,6-二羟基-4,5-二甲基-3-吡啶甲腈的钠盐。 2,6-二羟基-4,5-二甲基-3-吡啶腈的钠盐用氢溴酸水解,脱羧成2,6-二羟基-3,4-二甲基吡啶的氢溴酸盐。 所需的2,6-二羟基-3,4-二甲基吡啶由氢溴酸盐通过用氢氧化钠中和而产生。