Abstract:
Alkyl-H-phosphinic acid alkyl esters are synthesized in 65–71% yield via chemoselective reaction of alkyl bromides with available alkyl-H-phosphinic acids (60–65 °C, Et3N). The latter are prepared, in turn, by direct phosphorylation of alkyl bromides with red phosphorus under phase-transfer conditions.
Citation:
P. A. Volkov, K. O. Khrapova, A. A. Telezhkin, S. F. Malysheva, L. I. Larina, B. A. Trofimov, “Synthesis of alkyl-H-phosphinic acid alkyl esters from red phosphorus and alkyl bromides”, Mendeleev Commun., 32:6 (2022), 792–794
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https://www.mathnet.ru/eng/mendc801
https://www.mathnet.ru/eng/mendc/v32/i6/p792
This publication is cited in the following 1 articles:
S. F. Malysheva, V. A. Kuimov, S. N. Arbuzova, “Elemental Phosphorus in the Synthesis of Organophosphorus Compounds: The Recent Advances (A Review)”, Russ J Gen Chem, 93:S1 (2023), S238