A catalyst-free and expeditious general synthesis of N-benzyl-N-arylcyanamides under ultrasound irradiation at room temperature
Status PubMed-not-MEDLINE Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
31101288
DOI
10.1016/j.ultsonch.2019.04.038
PII: S1350-4177(19)30494-8
Knihovny.cz E-resources
- Keywords
- Benzyl bromide, Cyanamides, N-Benzyl-N-arylcyanamides, Ultrasound irradiation,
- Publication type
- Journal Article MeSH
A hitherto unknown, novel and direct approach to the efficient synthesis of N-benzyl-N-arylcyanamides is described via N-benzylation of a variety of arylcyanamides with benzyl bromide under ultrasound irradiation condition at room temperature; assorted N-benzyl-N-arylcyanamides are expeditiously accessible in excellent yields. The salient features of this approach include a very simple and clean reaction, higher yields obtained under mild conditions in an environmentally benign protocol. Additionally, easy isolation of the desired products without any tedious purification renders the present protocol a suitable alternative to desirable organic disubstituted cyanamides.
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