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Production of enolates of substituted alpha-ketoesters, comprises reaction of oxalic acid diesters with CH acid compounds in the presence of alcoholates using a 4-8C ether solvent
Production of enolates of substituted alpha-ketoesters, comprises reaction of oxalic acid diesters with CH acid compounds in the presence of alcoholates using a 4-8C ether solvent
Production of enolates of substituted alpha -ketoesters comprises reaction of oxalic acid diesters with CH acid compounds in the presence of alcoholates using a 4-8C ether solvent. Production of enolates of substituted alpha -ketoesters of formula (I) comprises reaction of oxalic acid diesters of formula (II) with CH acid compounds of formula (III) in the presence of alcoholates of formula MOR5 (4) using a 4-8C ether solvent. R1, R2 = H, COOR, C(O)R, CN, CONHR or CONR2; R = 1-20C alkyl (optionally branched or cyclic), 6-10C aryl or an aralkyl having an R group (alkyl and aryl groups are optionally substituted by heteroatoms); R3, R4 = R; M = alkali or alkaline earth metal; and R5 = alcoholic residue of an optionally branched or cyclic aliphatic 1-6C monoalcohol; Provided that both R1 and R2 are not H.
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机译:取代的α-酮酸酯的烯醇化物的生产包括在醇化物存在下使用4-8C醚溶剂使草酸二酯与CH酸化合物反应。式(I)的取代的α-酮酸酯的烯醇化物的制备包括在式MOR 5(4)的醇化物存在下,用式4使式(II)的草酸二酯与式(III)的CH酸化合物反应。 -8C乙醚溶剂。 R 1,R 2 = H,COOR,C(O)R,CN,CONHR或CONR 2; R = 1-20C烷基(任选地分支或环状),6-10C芳基或具有R基团的芳烷基(烷基和芳基任选地被杂原子取代); R 3,R 4 = R; M =碱金属或碱土金属; R 5 =任选地支链或环状的脂族1-6C一元醇的醇残基;假设R 1和R 2都不为H。
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