An Improved Synthesis of Ethyl Azodicarboxylate and 1,2,4-Triazoline-3,5-Diones Using Hypervalent Iodine Oxidation
- 1 March 1987
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 17 (4) , 409-413
- https://doi.org/10.1080/00397918708063918
Abstract
ARSTRACT: Hypervalent iodine oxidstion of 1,2-dicarhethoxy hydrazine (1) and 4-substituted urazoles (3) using iodobenzene diacetate or pentafluoroiodobenzene bis-trifluoroacetate in CH2Cl2 at room temperature proceeds smoothly to yield ethyl azodicarboxylate (2) and 4-substituted 1,2,4-triazoline-3,5-diones (4) in excellent yields.Keywords
This publication has 5 references indexed in Scilit:
- The Reaction of Silyl Enol Ethers With Ethyl Azodicarboxylate and 4-Phenyl-1,2,4-Triazoline-3,5-DioneSynthetic Communications, 1985
- Perfluoracyloxy‐Verbindungen des positiven JodsEuropean Journal of Inorganic Chemistry, 1967
- An Improved Synthesis of 1,2,4-Triazoline-3,5-dionesThe Journal of Organic Chemistry, 1966
- The Reaction of Ethyl Azodicarboxylate with Conjugated Dienes1The Journal of Organic Chemistry, 1962
- Über die Darstellung und Reaktionen von Azo‐acyl‐VerbindungenEuropean Journal of Inorganic Chemistry, 1912