Chloromethyl derivatives of 3-furyl-3-(diethoxyphosphoryl)acrylic acids
- Authors: Pevzner L.M.1
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Affiliations:
- St. Petersburg State Institute of Technology (Technical University)
- Issue: Vol 86, No 8 (2016)
- Pages: 1864-1870
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/215948
- DOI: https://doi.org/10.1134/S1070363216080156
- ID: 215948
Cite item
Abstract
Methoxymetyl derivatives of furoylphosphonates react with ethoxymethylenetriphenylphosphoranes to give phosphorylated (methoxymethylfuryl)acrylates. The reaction proceeds stereoselectively: phosphoryl and ester groups at the double bond are always trans-located. Treatment with dichloromethylmethyl ether and catalytic amount of zinc chloride converts the methoxymethyl group in the synthesized compounds into chloromethyl one. The ester group and the double bond are inert under these conditions.
About the authors
L. M. Pevzner
St. Petersburg State Institute of Technology (Technical University)
Author for correspondence.
Email: pevzner_lm@list.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013