2005Hecheng huaxueRequires access

Synthesis of 2-(β-Naphthoxymethyl)-5-aryl-1,3,4-oxadiazoles

Dejiang Li

Open publisher page 0 citations

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.

About this research paper

What this paper is about

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.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available 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.

Key concepts: Chemistry, Hydrazide, Elemental analysis, Aryl, Proton NMR, Ethanol, Organic chemistry, Nuclear chemistry

Back to paper searchBrowse research topicsOriginal source
Synthesis of 2-(β-Naphthoxymethyl)-5-aryl-1,3,4-oxadiazoles — Research Paper | ScholarLens