Issue 48, 2016

One-stage synthesis of FcP(O)(OC2H5)2 from ferrocene and α-hydroxyethylphosphonate

Abstract

A new approach is proposed for ferrocene phosphorylation using α-hydroxylalkylphosphonate as a “masked” phosphorylating agent, by electrochemical reduction of a ferrocene and (Me)2C(OH)P(O)(OC2H5)2 mixture at −50 °C. The method makes it possible to obtain the product of diethyl ferrocenyl phosphonate with a high yield (87–89%) and 100% conversion of the initial phosphonate in one stage. It is evidenced with experiments that ferrocene reduction is carried out with preservation of the iron charge in the ferrocene fragment and with the formation of a cyclopentadienyl ligand radical anion at −3.3 V ref. Ag/AgCl (at −50 °C).

Graphical abstract: One-stage synthesis of FcP(O)(OC2H5)2 from ferrocene and α-hydroxyethylphosphonate

Article information

Article type
Paper
Submitted
19 Feb 2016
Accepted
21 Apr 2016
First published
25 Apr 2016
This article is Open Access
Creative Commons BY license

RSC Adv., 2016,6, 42701-42707

Author version available

One-stage synthesis of FcP(O)(OC2H5)2 from ferrocene and α-hydroxyethylphosphonate

M. Khrizanforov, S. Strekalova, K. Kholin, V. Khrizanforova, V. Grinenko, T. Gryaznova and Y. Budnikova, RSC Adv., 2016, 6, 42701 DOI: 10.1039/C6RA04480H

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