Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol

I. S. Nizamov; D. A. Terenzhev; I. D. Nizamov; G. G. Shumatbaev; E. S. Batyeva; R. A. Cherkasov

doi:10.1134/S1070363216030117

Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol

Autores: Nizamov I.S.¹^,2, Terenzhev D.A.¹, Nizamov I.D.¹, Shumatbaev G.G.¹, Batyeva E.S.², Cherkasov R.A.¹
Afiliações:
1. Kazan Federal University
2. Arbuzov Institute of Organic and Physical Chemistry
Edição: Volume 86, Nº 3 (2016)
Páginas: 564-569
Seção: Article
URL: https://journals.rcsi.science/1070-3632/article/view/214191
DOI: https://doi.org/10.1134/S1070363216030117
ID: 214191

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Carvacrol trimethylsilyl ether when reacting with P₄S₁₀ forms S-trimethylsilyl ester of O,O-bis(5-isopropyl-2-methylphenyl)dithiophosphoric acid. The reactions of 2,4-diorganyl-1,3,2,4-dithiadiphosphetane-2,4-disulfides with carvacrol (thymol) trimethylsilyl ether yield the S-trimethylsilyl esters of the corresponding dithiophosphoric acids.