Direct C≡C Triple Bond Formation from the C=C Double Bond and Direct Hydroxylation into the o-Position of a Nitro Group on the Benzene Nucleus with Potassium t-Butoxide in N,N-Dimethylformamide in the Air^♯
Direct C≡C Triple Bond Formation from the C=C Double Bond and Direct Hydroxylation into the o-Position of a Nitro Group on the Benzene Nucleus with Potassium t-Butoxide in N,N-Dimethylformamide in the Air^♯
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DOI：
10.1246/bcsj.68.2043
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发表时间：
1995-07
影响因子：
4
通讯作者：
S. Akiyama;K. Tajima;S. Nakatsuji;K. Nakashima;K. Abiru;M. Watanabe
中科院分区：
文献类型：
--
作者：
S. Akiyama;K. Tajima;S. Nakatsuji;K. Nakashima;K. Abiru;M. Watanabe
A novel and facile method for direct C≡C acetylenic bond formation from the C=C double bond by treatment with potassium t-butoxide (t-BuOK) in N,N-dimethylformamide in the air has been found in a 9,10-bis(4-substituted styryl)anthracene series, in 4-substituted 4′-nitrostilbene series, and in 1-(p-nitrophenyl)-4-(p-substituted phenyl)-1,3-butadiene series; its scope and limitations have been examined. The ESR spectrum of the reaction against 4-diethylamino-4′ -nitrostilbene was measured to identify an anion radical species expected for explanation of the mechanism of the dehydrogenation reaction. Further, cyclic voltammetric measurements of a series of stilbenes and diphenylacetylenes were carried out in connection with the above mechanism. In many cases, interestingly, the use of a large excess of t-BuOK brought about succeeding hydroxylation into the ortho-position of a nitro group on the benzene nucleus. The simple hydroxylation is useful for the synthesis of substituted 5-(arylethynyl)-2-nitrophenols,...
