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γ-Ketosulfides and Hydroxysulfides from Sodium Methanthiolate of Sulfidic Spent Caustics
Abstract Condensation of pentan-3-one, hexan-2-one, 4-methylpentan-2-one, 5-methylhexan-3-one, or 2,6-dimethylheptan-4-one with formaldehyde and sodium methanethiolate, which is present in sulfidic spent caustic from the Orenburg gas processing plant, yields the corresponding mono- and bis[(methylsulfanyl)methyl]-substituted ketones or their mixtures depending on the reactant ketone structure. Alkylthiomethylation of butan-2-one with equimolar amounts of formaldehyde and sodium methanethiolate results in 3-methyl-5-thiahexan-2-one or, in the case of a twofold excess of the reagents, in 2-methyl-1,5-bis(methylsulfanyl)-4-[(methylsulfanyl)methyl]pentan-3-one. On the basis of 3-methyl-5-thiahexan-2-one, new polyfunctional [(methylsulfanyl)methyl]-substituted alcohol, α-hydroxymethylketone, 1,3-diol, and 1,3-dioxane have been obtained.
γ-Ketosulfides and Hydroxysulfides from Sodium Methanthiolate of Sulfidic Spent Caustics
Abstract Condensation of pentan-3-one, hexan-2-one, 4-methylpentan-2-one, 5-methylhexan-3-one, or 2,6-dimethylheptan-4-one with formaldehyde and sodium methanethiolate, which is present in sulfidic spent caustic from the Orenburg gas processing plant, yields the corresponding mono- and bis[(methylsulfanyl)methyl]-substituted ketones or their mixtures depending on the reactant ketone structure. Alkylthiomethylation of butan-2-one with equimolar amounts of formaldehyde and sodium methanethiolate results in 3-methyl-5-thiahexan-2-one or, in the case of a twofold excess of the reagents, in 2-methyl-1,5-bis(methylsulfanyl)-4-[(methylsulfanyl)methyl]pentan-3-one. On the basis of 3-methyl-5-thiahexan-2-one, new polyfunctional [(methylsulfanyl)methyl]-substituted alcohol, α-hydroxymethylketone, 1,3-diol, and 1,3-dioxane have been obtained.
γ-Ketosulfides and Hydroxysulfides from Sodium Methanthiolate of Sulfidic Spent Caustics
Baeva, L. A. (author) / Biktasheva, L. F. (author) / Fatykhov, A. A. (author) / Lyapina, N. K. (author)
Petroleum Chemistry ; 59 ; 615-621
2019-06-01
7 pages
Article (Journal)
Electronic Resource
English
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