Chem. J. Chinese Universities ›› 2000, Vol. 21 ›› Issue (S1): 486.
• Synthetic Sciences • Previous Articles Next Articles
LIU Wan-Yi2, XU Qi-Hai1, LIANG Yong-Min1, MA Yong-Xiang1
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Abstract:
Organometallic structure possessing extensively conjugated π-electron system are an interesting class of potentially highly nonlinear molecular blocks and photoactive semiconductor[1,2]. The title compounds were synthesized following Wittig reaction or palladium-catalyzed reaction of olefines and iodoferrocene, which proceed in solution and refluxing[3]. However, there are always some disadvantages such as long reaction time, difficult work-up and low yield. Herein we report a free-solvent synthesis of aryl and vinyl ferrocene derivatives. As shown in the table, the phosphoning salt (1mol),NaOH (1.5mol) and formylferrocene (1mol) were mixed by grinding at room temperature to 65℃ in dry state to give the corresponding title compounds in 60-90% yield. The reaction was usually completed within a few minutes. The product thus obtained is mainly E-isomer. It could be emphasized that solid-state Wittig reaction is fast, cleaner and efficient.
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LIU Wan-Yi, XU Qi-Hai, LIANG Yong-Min, MA Yong-Xiang. Solid-state Synthesis of Aryl and Vinyl of Ferrocene Derivatives via Wittig Reaction[J]. Chem. J. Chinese Universities, 2000, 21(S1): 486.
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http://www.cjcu.jlu.edu.cn/EN/Y2000/V21/IS1/486