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Percarboxylic acids prepn. from acid chlorides in soln. - using conc. hydrogen peroxide, opt. with pyridine

机译:过羧酸制备。从溶液中的酰氯中提取。 -使用浓。过氧化氢,选择。用吡啶

摘要

Prepn. of peroxycarboxylic acids is by reaction of conc. H2O2 on a carboxylic acid chloride in soln. in THF, diethyl ether or dioxan at -20 to +30 degrees C., opt. in the presence of pyridine. The H2O2 pref. has a concn. of =30 wt.%, esp. 85 wt.% and is usually used in excess, partic. in a molar ratio of approx. 2:1, based on wt. of acid chloride. The min. amt. of solvent required to dissolve the reactants is pref. used and pref. 0.5 mol. equiv. of pyridine are used when aliphatic acids are prod. and 0.125 mol. equiv. for other types. Prodn. of aliphatic, aromatic and substd. polycarboxylic acids is possible in high yields, e.g. 75-85%, without simultaneous prodn. of organic peroxides. Acidification of reaction mixt. is avoided thus allowing prepn. of percarboxylic acids with ester functions.
机译:准备过氧羧酸的缩合反应通过浓溶液中的羧酸氯化物上的过氧化氢。选择在-20至+30摄氏度下于THF,乙醚或二恶烷中制得。在吡啶存在下。 H2O2优选。有一个concn。 > = 30 wt。%,特别是85重量%,通常过量使用。摩尔比约为2:1,基于wt酰氯。分钟amt。溶解反应物所需的溶剂量优选。使用和偏好。 0.5摩尔当量当生产脂族酸时,使用吡啶。和0.125摩尔。当量对于其他类型。产品脂肪族,芳香族和取代基。多羧酸是可能的,例如以高收率得到。 75-85%,无同步产品。有机过氧化物。反应混合物酸化。避免因此允许prepn。具有酯功能的过羧酸。

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