Convenient Synthesis and Free-Radical Copolymerization of p-Chloromethylstyrene
- 1 August 1979
- journal article
- research article
- Published by Taylor & Francis in Journal of Macromolecular Science: Part A - Chemistry
- Vol. 13 (6), 767-775
- https://doi.org/10.1080/00222337908056687
Abstract
P-Chloromethylstyrene, a useful monomer for a starting material in preparation of functional polymers, is conveniently synthesized by the chloromethylation of 2-phenyl-ethyl bromide followed by dehydrobromination. This procedure is simpler and the yield is higher than those of methods previously described. Radical copolymerizations of this compound with styrene and methyl methacrylate were studied at 60°C. From the copolymerization with styrene, Q and e values for p-chloromethylstyrene were calculated as Q = 1.13 and e = −0.58. Similarly, the copolymerization parameters with methyl methacrylate were obtained as Q = 1.16 and e = −0.69.Keywords
This publication has 5 references indexed in Scilit:
- The use of insoluble polymer supports in organic chemical synthesisChemical Society Reviews, 1974
- Reactions on PolymersPublished by Springer Nature ,1973
- Syntheses ofp-Vinylbenzyl Ethers and p-Vinylbenzyl Sulfides and Their PolymerizationsJournal of Synthetic Organic Chemistry, Japan, 1969
- Chloromethylation of PolystyreneIndustrial & Engineering Chemistry, 1952
- Higher Hydrocarbons.1 III.2 The Wolff-Kishner ReactionJournal of the American Chemical Society, 1945