406913-23-3Relevant academic research and scientific papers
Direct conversion of N-ethylamines into functionalised amides by S2Cl2
Konstantinova,Rakitin,Rees
, p. 167 - 168 (2001)
Hünig's base 1 is known to react extensively with S2Cl2 to give monocyclic, bicyclic and fused tricyclic 1,2-dithioles with the N-ethyl group intact, but with S2Cl2 and DABCO in chloroform at 0 °C 1 is converted
Transformations of N-ethylamines into amide derivatives under the action of sulfur monochloride
Konstantinova,Berezin,Rakitin
, p. 1178 - 1183 (2008/09/19)
Tertiary N-ethylamines were converted into amide derivatives by reactions with sulfur monochloride and DABCO at 0 °C. Depending on the nature of the substituents in the amine, the reaction can be accompanied by unexpected transformations.
