Synthesis of new monomers and polymers. II. 3-methyl-5-isopropenylpyrazoles and derivatives
✍ Scribed by Dufonteny, L. ;Mifuna, E. ;Neirynck, G. ;Teyssié, Ph.
- Book ID
- 104532063
- Publisher
- John Wiley and Sons
- Year
- 1962
- Weight
- 566 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0022-3832
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The synthesis of 3‐methyl‐5‐isopropenylpyrazole and 1‐phenyl‐3‐methyl‐5‐isopropenylpyrazole is described, as well as the isolation of an addition compound with vinyl isocyanate, namely the N‐vinyl‐1‐(3‐methyl‐5‐isopropenylpyrazolyl)carboxamide. The 3‐methyl‐5‐isopropenylpyrazole only is able to homopolymerize, giving a characteristic polyelectrolyte, but both pyrazoles copolymerize readily with acrylic acid to yield polyampholytes. The addition compound, whose structure is proved by several methods, polymerizes readily; the soluble product obtained may undergo a grafting reaction with other monomers, but the polymer obtained is highly crosslinked.
📜 SIMILAR VOLUMES
2-Hydroxymethyl-but-1-ene-3-one [␣-hydroxymethyl methyl vinyl ketone (HMVK)] was synthesized from methyl vinyl ketone using paraformaldehyde and a tertiary amine catalyst. Free-radical polymerization of this monomer created transparent, tough polymers that were insoluble in organic solvents. HMVK wa
## Abstract By condensation of polyvinylamine with several aromatic aldehydes, poly‐Schiff bases were obtained, which were practically 100% pure. The polysalicylidenevinylamine and its 5‐chloro‐, 5‐nitro, 4‐hydroxy, and 3‐methoxy derivatives, as well as the poly‐2‐hydroxynaphthylidenevinylamine and