Oxidation of Alcohols with<i>t</i>-Butyl Chromate. III. The Oxidation of Alicyclic Alcohols
作者:Takayuki Suga、Tamon Matsuura
DOI:10.1246/bcsj.38.1503
日期:1965.9
1) The t-butyl chromate oxidation of myrtenol gave no ester, but it did give the corresponding aldehyde as the main product, while the oxidation of cyclohexylcarbinol gave a mixture of the corresponding aldehyde, acid and ester in comparable yields. 2) A similar oxidation of cyclohexanol afforded the corresponding ketone in a high yield, while the oxidation of cyclohexane-trans-1,2-diol produced no
1) 桃金娘醇的铬酸叔丁酯氧化没有产生酯,但它确实产生了相应的醛作为主要产物,而环己基甲醇的氧化产生了相应的醛、酸和酯的混合物,产率相当。2)环己醇的类似氧化以高产率提供相应的酮,而环己烷-反式-1,2-二醇的氧化不产生相应的二酮,但确实产生了乙二醇裂变产物和环酯,如反式- 1,2-己二氧基环己烷(一种新化合物)。另一方面,对薄荷烷-反式-3,4-二醇仅以良好的产率产生相应的羟基酮。