One-Pot Synthesis of Dialkyl 2-[(2,5-Dioxo-1-pyrrolidinyl)- oxy]-2-butenedioates from Acetylenic Esters and n-Hydroxysuccinimide
Corresponding Author(s) : ALI REZA KAZEMIZADEH
alirezakazemizadeh@yahoo.com
Asian Journal of Chemistry,
Vol. 19 No. 7 (2007): Vol 19 Issue 7
Abstract
A one-pot synthesis of electron-poor O-vinyl pyrrolidine in fairly high yields by the reaction of N-hydroxysuccinimide and dialkyl acetylenedicarboxylates in water-acetone media is reported. The structures of these compounds were confirmed by IR, 1H and 13C NMR spectroscopy. The NMR spectra indicated that E- and Z-isomers of the products are formed.
Keywords
Acetylenic esters
N-Hydroxysuccinimide
Environment-friendly
Michael addition
O-Vinylation
REZA KAZEMIZADEH, A., & RAMAZANI AND BIJAN GANJEIE, A. (2010). One-Pot Synthesis of Dialkyl 2-[(2,5-Dioxo-1-pyrrolidinyl)- oxy]-2-butenedioates from Acetylenic Esters and n-Hydroxysuccinimide. Asian Journal of Chemistry, 19(7), 5784–5786. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/13204
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