1587-26-4Relevant articles and documents
Orientation in Base-Promoted Dehydrochlorination of 2,2,3-Trichlorobutane
Bartsch, Richard A.,Croft, Alan P.
, p. 1364 - 1365 (1982)
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INVESTIGATION IN THE FIELD OF UNSATURATED COMPOUNDS VI. LIQUID-PHASE CHLORINATION OF 2-HALOGENO-2-BUTENES
Mkryan, G. G.,Kaplanyan, E. E.,Mkryan, G. M.
, p. 1833 - 1836 (2007/10/02)
The liquid-phase chlorination of 2-halogeno-2-butenes in the presence of tert-butylpyrocatechol leads to the formation of the products from an anomalous reaction (2,3-dihalogeno-1-butenes), substitution of hydrogen at the double bond (2,3-dihalogeno-2-butenes), and normal addition (2,2,3-trihalogenobutanes).The ratios of these compounds are 70:6:24 in the case of 2-chloro-2-butene and 54:7.5:38.5 in the case of 2-bromo-2-butene.During the chlorination of 2-chloro-2-butene in the presence of sodium bicarbonate the formation of 3-chloro-2-butanol (20percent) was observed as a result of the combined addition of chlorine and water.