Alkylation of CH acids with haloidalkyl-1,3-dioxolanes
- Authors: Raskil’dina G.Z.1, Borisova Y.G.1, Spirikhin L.V.1, Zlotsky S.S.1
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Affiliations:
- Ufa State Petroleum Technological University
- Issue: Vol 87, No 5 (2017)
- Pages: 1097-1100
- Section: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/220098
- DOI: https://doi.org/10.1134/S1070363217050358
- ID: 220098
Cite item
Abstract
Alkylation of diethyl malonate and Meldrum acid with haloalkyl-1,3-dioxolanes has afforded the substituted malonates; their decarboxylation has led to the formation of esters containing a cycloacetal fragment. Reactions of the substituted malonates with urea have yielded the corresponding substituted barbiturates. Monodecarboxylation of the obtained malonates has led to the formation of 1,3-dioxolane-carboxylates.
About the authors
G. Z. Raskil’dina
Ufa State Petroleum Technological University
Author for correspondence.
Email: graskildina444@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062
Yu. G. Borisova
Ufa State Petroleum Technological University
Email: graskildina444@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062
L. V. Spirikhin
Ufa State Petroleum Technological University
Email: graskildina444@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062
S. S. Zlotsky
Ufa State Petroleum Technological University
Email: graskildina444@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062