One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment-Reference-Cited by-同舟云学术

One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment

Published:2021 Issue:39 Volume:11 Page:24232-24237
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Lin Hongyan¹²³⁴⁵^ORCID,Zhou Ziling¹²³⁴⁵,Ma Xiaopeng¹²³⁴⁵,Chen Qingqing¹²³⁴⁵,Han Hongwei¹²³⁴⁵,Wang Xiaoming¹²³⁴⁵^ORCID,Qi Jinliang¹²³⁴⁵,Yang Yonghua¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratory of Pharmaceutical Biotechnology

2. Institute of Plant Molecular Biology

3. School of Life Sciences

4. Nanjing University

5. Nanjing 210023

Abstract

In a formic acid–H₂O solution (60% : 40%), most aromatic aldehydes react efficiently with hydroxylamine hydrochloride and sodium acetate to form nitriles, where formic acid acts as both catalyst and solvent.

Funder

National Natural Science Foundation of China

Central University Basic Research Fund of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/RA/D1RA03559B

Reference23 articles.

1. Difluorocarbene-Based Cyanation of Aryl Iodides

2. Vapour phase ammoxidation of toluene over vanadium oxide supported on Nb2O5–TiO2

3. Recent developments and perspectives in palladium-catalyzed cyanation of aryl halides: synthesis of benzonitriles

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