| Autor: |
Nikonova, V. S., Kaliev, A. R., Borodina, T. N., Smirnov, V. I., Rozentsveig, I. B., Korchevin, N. A. |
| Předmět: |
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| Zdroj: |
Russian Journal of Organic Chemistry; Dec2019, Vol. 55 Issue 12, p1912-1917, 6p, 5 Diagrams, 1 Chart |
| Abstrakt: |
A green approach was proposed for the synthesis of 2-chloroprop-2-en-1-yl sulfones in 47–94% yield. The molecular and crystal structures of 2-chloroprop-2-en-1-yl phenyl sulfone and 2-chloroprop-2-en-1-yl methyl sulfone were determined by X-ray analysis. π-Stacking interaction between the benzene ring and double bond was revealed in the crystal structure of 2-chloroprop-2-en-1-yl phenyl sulfone. Chloropropenyl sulfones were found to readily undergo dehydrochlorination to give stable allenyl sulfones and alkaline hydrolysis to produce the corresponding acetonyl sulfones. The latter can be converted to oximes by treatment with hydroxylamine hydrochloride. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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