Synthesis of Monosubstituted Derivatives of 4,5-Dichlorophthalonitrile in a DMF–Water System

A simple procedure was developed for the synthesis of undescribed 4-aryloxy-5-chlorophthalonitriles and 4-arylsulfanyl-5-chlorophthalonitriles by SNAr reaction of 4,5-dichlorophthalonitrile with phenols and thiophenols in a DMF–water binary solvent. The resulting ortho-dicarbonitriles are of interest as precursors for the synthesis of phthalocyanines. The product yields ranged from 30 to 59%.

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Publication Details

Journal
Russian Journal of General Chemistry
Published
2024-11-01
DOI
https://doi.org/10.1134/s1070363224110069
Citations
1
Primary Topic
Synthesis and Reactions of Organic Compounds
Type
article
Field-Weighted Citation Impact
0.25
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article

Synthesis of Monosubstituted Derivatives of 4,5-Dichlorophthalonitrile in a DMF–Water System

A. E. Rassolova, V. V. Bukhalin, V. V. Aleksandriiskii, V. L. Baklagin et al.
1 citations
Russian Journal of General Chemistry
Synthesis and Reactions of Organic Compounds
0.25
article

Synthesis of Monosubstituted Derivatives of 4,5-Dichlorophthalonitrile in a DMF–Water System

A. E. Rassolova, V. V. Bukhalin, V. V. Aleksandriiskii, V. L. Baklagin, И. Г. Абрамов, В. Е. Майзлиш
article en
1 citations

Abstract

A simple procedure was developed for the synthesis of undescribed 4-aryloxy-5-chlorophthalonitriles and 4-arylsulfanyl-5-chlorophthalonitriles by SNAr reaction of 4,5-dichlorophthalonitrile with phenols and thiophenols in a DMF–water binary solvent. The resulting ortho-dicarbonitriles are of interest as precursors for the synthesis of phthalocyanines. The product yields ranged from 30 to 59%.

Russian Journal of General ChemistryVol. 94(11)
Ivanovo State University (RU), Yaroslavl State Technical University (RU)
Clean water and sanitation
Openalex Percentile: Top 45%
Synthesis and Reactions of Organic Compounds
0.25
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