Chem. J. Chinese Universities ›› 1993, Vol. 14 ›› Issue (5): 642.

• Articles • Previous Articles     Next Articles

Isomerization/Chlorination of S-Alkyl(Aryl)O,O-dialkyl Dithiophosphate ——A New Method for Synthesis of S-Alkyl S-Alkyl(Aryl) Dithiophosphoric Acid Derivatives

TANG Chu-Chi, WU Gui-Ping   

  1. Institute of Elemento-Organic Chemistry, Nankai University, Tianjin, 300071
  • Received:1992-05-18 Revised:1993-02-18 Online:1993-05-24 Published:1993-05-24

Abstract: Eleven compounds, among which nine are new compounds, of S-alkyl S-alkyl (aryl) dithiophosphpric acid derivatives have been synthesized by using a new convenient method which is based on the isomerization/chlorination of S-alkyl (aryl) O,O-dialkyl dithiophosphate with phosphorus oxychloride to give S-alkyl S-alkyl (aryl) phosphorochloridodithiolate.Then, this phosphorochlo-ridodithiolate reacts with various nuclosphiles, such as alcohol, phenol, mercaptan, thiophenol, ammonia in the presence of acid-binding agent to obtain S-alkyl S-alkyl (aryl) dithiophosphoric acid derivatives, such as S-alkyl S-alkyl (aryl) O-alkyl(aryl) phosphorodithiolate, S-alkyl S,S-dialkyl (aryl) phosphorotrithiolate, S-alkyl S-alkyl (aryl) phosphoramidodithiolate.The results of the tests in biological activity show that these compounds prepared possess a certain insecticidal or fungicidal activ-itiy.

Key words: Phosphorodithiolate, Phosphorotrithiolate, Phosphoramidodithiolate, Chlorination, Iso-merization

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