Scalable, safer and greener syntheses of vinylimidazoles via reactive distillation of hydroxyethylimidazole intermediates. Issue 5 (1st January 2021)
- Record Type:
- Journal Article
- Title:
- Scalable, safer and greener syntheses of vinylimidazoles via reactive distillation of hydroxyethylimidazole intermediates. Issue 5 (1st January 2021)
- Main Title:
- Scalable, safer and greener syntheses of vinylimidazoles via reactive distillation of hydroxyethylimidazole intermediates
- Authors:
- Alshaikh, Ali
O'Harra, Kathryn E
Liu, Xiaoyang
Whitley, John W
Mittenthal, Max S
Taylor, Wesley F
Turner, C Heath
Bara, Jason E - Abstract:
- Abstract: 1‐Vinylimidazole has been extensively utilized by the polymer science community, due to its high reactivity for free radical polymerization and the variety of uses for both neutral polyvinylimidazole and cationic polyvinylimidazolium forms. While much rarer, 4‐vinylimidazoles and 2‐vinylimidazoles are less synthetically accessible. In comparison to conventional methods for the synthesis of vinylimidazole derivatives from energy‐intensive reaction conditions utilizing hazardous, gaseous precursors, herein we demonstrate a simple and versatile two‐step method applied to the synthesis of seven 1‐vinylimidazoles with different substituents as well as an initial demonstration of a facile method to synthesize the rare compound 1‐methyl‐2‐vinylimidazole. The process relies upon the synthesis of N ‐hydroxyethylimidazole precursors via a ring‐opening reaction from substituted imidazoles with ethylene carbonate, a 'green' substance formed from CO2 and ethylene oxide. For the synthesis of 1‐methyl‐2‐vinylimidazole, the hydroxyethylimidazole intermediate is conveniently formed from 1, 2‐dimethylimidazole and paraformaldehyde. These hydroxyethylimidazoles are subsequently dehydrated to the corresponding 1‐ or 2‐vinylimidazole forms using a base‐catalyzed reactive distillation. The optimization of process conditions is discussed, and properties of the vinylimidazole derivatives were computationally studied using density functional theory calculations. This work reveals scalableAbstract: 1‐Vinylimidazole has been extensively utilized by the polymer science community, due to its high reactivity for free radical polymerization and the variety of uses for both neutral polyvinylimidazole and cationic polyvinylimidazolium forms. While much rarer, 4‐vinylimidazoles and 2‐vinylimidazoles are less synthetically accessible. In comparison to conventional methods for the synthesis of vinylimidazole derivatives from energy‐intensive reaction conditions utilizing hazardous, gaseous precursors, herein we demonstrate a simple and versatile two‐step method applied to the synthesis of seven 1‐vinylimidazoles with different substituents as well as an initial demonstration of a facile method to synthesize the rare compound 1‐methyl‐2‐vinylimidazole. The process relies upon the synthesis of N ‐hydroxyethylimidazole precursors via a ring‐opening reaction from substituted imidazoles with ethylene carbonate, a 'green' substance formed from CO2 and ethylene oxide. For the synthesis of 1‐methyl‐2‐vinylimidazole, the hydroxyethylimidazole intermediate is conveniently formed from 1, 2‐dimethylimidazole and paraformaldehyde. These hydroxyethylimidazoles are subsequently dehydrated to the corresponding 1‐ or 2‐vinylimidazole forms using a base‐catalyzed reactive distillation. The optimization of process conditions is discussed, and properties of the vinylimidazole derivatives were computationally studied using density functional theory calculations. This work reveals scalable synthetic methods for previously inaccessible vinylimidazole compounds which can enable the design of new polymers. © 2020 Society of Chemical Industry Abstract : The synthesis of 1‐vinylimidazoles and 2‐vinylimidazoles via reactive distillation of hydroxyethylimidazole intermediates offers a scalable, safer and greener method to produce these monomers and expand applications of polyvinylimidazole materials. … (more)
- Is Part Of:
- Polymer international. Volume 70:Issue 5(2021)
- Journal:
- Polymer international
- Issue:
- Volume 70:Issue 5(2021)
- Issue Display:
- Volume 70, Issue 5 (2021)
- Year:
- 2021
- Volume:
- 70
- Issue:
- 5
- Issue Sort Value:
- 2021-0070-0005-0000
- Page Start:
- 582
- Page End:
- 593
- Publication Date:
- 2021-01-01
- Subjects:
- reactive distillation -- vinylimidazole -- N‐heterocyclic monomers -- glycerol -- ethylene carbonate
Plastics -- Periodicals
Polymers -- Periodicals
Polymerization -- Periodicals
547.7 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/pi.6161 ↗
- Languages:
- English
- ISSNs:
- 0959-8103
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.706750
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 16182.xml