Synthesis of 2-(β-Naphthoxymethyl)-5-aryl-1,3,4-oxadiazoles
Dejiang Li
Abstract
Dejiang Li
Abstract
2-β-Naphthoxymethyl)-5-aryl-1,3,4-oxadiazoles were prepared from hydrazide, which were converted with acylchloride in ethanol into N-substituted hydrazide, followed by treatment with phosphorous oxychloride. Their structrues were characterized by 1H NMR, IR, MS and elemental analysis.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
2-β-Naphthoxymethyl)-5-aryl-1,3,4-oxadiazoles were prepared from hydrazide, which were converted with acylchloride in ethanol into N-substituted hydrazide, followed by treatment with phosphorous oxychloride. Their structrues were characterized by 1H NMR, IR, MS and elemental analysis.
Key concepts: Chemistry, Hydrazide, Elemental analysis, Aryl, Proton NMR, Ethanol, Organic chemistry, Nuclear chemistry