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Diels-Alder reaction of cyclopentadiene with non-polar acrylic acid - on the surface of solid particles with subsequent elution of adduct with organic solvent

机译:环戊二烯与非极性丙烯酸的Diels-Alder反应-在固体颗粒表面,随后用有机溶剂洗脱加合物

摘要

Reaction of cyclopentadiene with alpha,beta-unsatd. organic cpds. by the Diels-Alder reaction and then recovery of the resulting adduct, is carried out between non-polar, opt. substd. acrylic acid derivs. and the cyclopentadiene in heterogeneous phase on specific surfaces of solid particles, and the endo- and/or exo-adducts are eluted from the solid surfaces with known organic solvents. Prodn. of 2-norbornene-5-carboxylic acid derivs. suitable for use in further chemical reactions such as hydrogenation reactions, rearrangements and substitution reactions. The prods. are intermediates for biologically active cpds. such as herbicides and fungicides. Simple and easy-to-perform process suitable for continuous operation. The process gives reproducible results, and process conditions can be varied to reproducibly favour production of either the exo- or the endo- isomer.
机译:环戊二烯与α,β-不饱和基的反应有机cpds。通过Diels-Alder反应,然后回收生成的加合物,在非极性之间进行。取代丙烯酸衍生。在固体颗粒的特定表面上形成异相的环戊二烯,并且用已知的有机溶剂从固体表面上洗脱内和/或外加合物。产品2-降冰片烯-5-羧酸衍生物。适用于进一步的化学反应,例如氢化反应,重排和取代反应。刺。是具有生物活性的cpds的中间体。如除草剂和杀菌剂。简单且易于执行的过程适合连续操作。该方法可提供可重复的结果,并且可以改变工艺条件以可重复地有利于外向异构体或内向异构体的生产。

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