Synthesis of Phosphine Chalcogenides Using Tetrabutylammonium Chalcogenocyanates

The new chalcogenylation of phosphines using <sup>n</sup>Bu<sub>4</sub>N‧XCN (X = S, Se) is described. The reaction in 1,2-dichloroethane at 120 °C provided the corresponding phosphine sulfides in good to high yields. The protocol could be extended to the synthesis of phosphinic acid derivatives as well as sulfurization of poly(styrene-co-4-styryldiphenylphosphine).

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Publication Details

Journal
Chemical and Pharmaceutical Bulletin
Published
2024-08-21
DOI
https://doi.org/10.1248/cpb.c24-00372
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of Phosphine Chalcogenides Using Tetrabutylammonium Chalcogenocyanates

Masahiro Anada, Azumi Watanabe, Shunsuke Sueki, Takeo Suga et al.
Chemical and Pharmaceutical Bulletin
Organophosphorus compounds synthesis
article

Synthesis of Phosphine Chalcogenides Using Tetrabutylammonium Chalcogenocyanates

Masahiro Anada, Azumi Watanabe, Shunsuke Sueki, Takeo Suga, Kosho Makino, Naoyuki Machida, Shuhei Abe, Minori Nakamura
article en

Abstract

The new chalcogenylation of phosphines using <sup>n</sup>Bu<sub>4</sub>N‧XCN (X = S, Se) is described. The reaction in 1,2-dichloroethane at 120 °C provided the corresponding phosphine sulfides in good to high yields. The protocol could be extended to the synthesis of phosphinic acid derivatives as well as sulfurization of poly(styrene-co-4-styryldiphenylphosphine).

Chemical and Pharmaceutical BulletinVol. 72(8)
Waseda University (JP), Musashino University (JP)
Musashino University, Seikei University, Inamori Foundation, Japan Society for the Promotion of Science
Openalex Percentile: Top 90%
Organophosphorus compounds synthesis
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Synthesis of Phosphine Chalcogenides Using Tetrabutylammonium Chalcogenocyanates — Masahiro Anada, Azumi Watanabe, et al. · Chemical and Pharmaceutical Bulletin (2024) | TGRS Research Map | TGRS