Synthesis and Wittig Reaction of Formylated (Trifluoromethylfuryl)methanephosphonates


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Abstract

Methods of synthesis of 4-functionalyzed (5-trifluoromethylfur-2-yl)methanephosphonates and (5-methyl-2-trifluoromethylfur-3-yl)methanephosphonate are developed. Their formylation with ethyl formate in the presence of sodium foil is studied. Spectral characteristics of tautomers of obtained derivatives of phosphonoacetic aldehyde are evaluated. It is shown that interaction of obtained formyl derivatives with ethoxycarbonylmethylenetriphenylphosphorane regardless of the structure of the furan fragment leads to 4-furylsubstituted alkyl 4-(diethoxyphosphoryl)but-3-enoate, the abnormal product of Wittig reaction.

About the authors

E. P. Doronina

St. Petersburg Institute of Technology (Technical University)

Email: pevzner_lm@list.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013

L. M. Pevzner

St. Petersburg Institute of Technology (Technical University)

Author for correspondence.
Email: pevzner_lm@list.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013

V. A. Polukeev

Institute of Experimental Medicine

Email: pevzner_lm@list.ru
Russian Federation, St. Petersburg

M. L. Petrov

St. Petersburg Institute of Technology (Technical University)

Email: pevzner_lm@list.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013


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