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    • 3. 发明授权
    • Process for preparing carboxylic acid esters of dicyclopentadienes
    • 二环戊二烯羧酸酯的制备方法
    • US4390717A
    • 1983-06-28
    • US257152
    • 1981-04-24
    • Katuhiro IshikawaRyotaro OhnoMasatoshi Arakawa
    • Katuhiro IshikawaRyotaro OhnoMasatoshi Arakawa
    • B01J23/00B01J31/00C07C67/38C07C69/753
    • C07C67/38C07C2103/68
    • A process for preparing a carboxylic acid ester of a dicyclopentadiene by reacting the dicyclopentadiene with carbon monoxide and an alcohol in the presence of a cobalt compound catalyst, characterized by carrying out said reaction in the presence of 0.5 mole or more of a pyridine base per mole of the dicyclopentadiene at a temperature of 130.degree. C. or less at a carbon monoxide pressure of preferably at least 20 kg/cm.sup.2. G to hydroesterify the double bond in the norbornene ring, thereby forming a mono-carboxylate of a dicyclopentadiene, and hydroesterifying the monoesterification product as produced or the isolated monoester to the same reaction conditions as above except that the temperature is 160.degree. C. or less to hydroesterify the remaining double bond of the monoester, thereby forming a dicarboxylate of dicyclopentadiene.
    • 一种通过在钴化合物催化剂存在下使二环戊二烯与一氧化碳和醇反应制备二环戊二烯的羧酸酯的方法,其特征在于在0.5摩尔或更多的吡啶碱存在下进行所述反应,每摩尔 的二环戊二烯在130℃或更低的温度下,优选至少20kg / cm2的一氧化碳压力。 G将降冰片烯环中的双键加成酯化,从而形成二环戊二烯的单羧酸酯,并将所生产的单酯化产物或分离的单酯加氢酯化至与上述相同的反应条件,除了温度为160℃或更低 以使单酯的剩余双键加氢酯化,从而形成二环戊二烯的二羧酸酯。