Solvent Incorporation in Bromination of Acetylenes in Alcohols
- 1 June 1978
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 51 (6) , 1911-1912
- https://doi.org/10.1246/bcsj.51.1911
Abstract
The reactions of acetylenes with bromine in alcohols at 20–25 °C afford dibromodialkoxyalkanes in good yields together with variable amounts of dibromoalkenes. Similar treatment of phenylacetylene with copper(II) bromide gives only bromophenylacetylene and 2-phenyl-1,1,2-tribromoethylene, the latter being formed by dibromination of the former with copper(II) bromide.This publication has 4 references indexed in Scilit:
- N-Bromosuccinimide-Induced Dimethyl Sulfoxide Oxidation of AcetylenesCanadian Journal of Chemistry, 1971
- Polar addition of molecular fluorine to acetylenesThe Journal of Organic Chemistry, 1967
- Cupric Halide HalogenationsThe Journal of Organic Chemistry, 1965
- Halogenation of 1-Hexyne in Methanol1Journal of the American Chemical Society, 1938