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METHOD OF 2-(TETRAHYDRO-2-FURFURYL)-3-(1-NAPHTHYL)-PROPANOIC ACID PREPARATION

机译:2-(四氢-2-呋喃基)-3-(1-萘基)-丙酸的制备方法

摘要

Solution concerns the method of the preparation of 2-/tetrahydro-2-furfuryl/-3-/1-naftyl/propanoic acid of formula I by alkaline hydrolysis of dialkyl esters of 1-/tetrahydro-2-furyl/-3-/1-naftyl-2.2-propandicarboxylic acid of the general formula III, in which R means methyl or ethyl group and subsequent thermic decarboxylation of corresponding alkaline salts and/or of dicarboxylic acid of the general formula II, in which R1 means the atom of sodium, potassium, or hydrogen in mineral acid and in an aprotic solvent. The solution makes it possible to execute a one-step synthesis of the required substance of the formula I, without isolation of intermediate products. The substance of the formula I serves as an intermediate product in the preparation of pharmaceutical with vasodilatative and nootropic effects in human medicineIMAGE
机译:溶液涉及通过碱性水解1- /四氢-2-糠基/ -3- /的二烷基酯来制备式I的2- /四氢-2-糠基/ -3- / 1-萘基/丙酸的方法。通式III的1-萘基-2.2-丙二羧酸,其中R表示甲基或乙基,以及随后相应的碱性盐和/或通式II的二羧酸的热脱羧,其中R 1表示无机酸和非质子溶剂中钠,钾或氢的原子。该解决方案使得有可能进行式I的所需物质的一步合成,而无需分离中间产物。式I的物质在制备具有人类血管舒张作用和促智作用的药物中用作中间体。

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