2-(Multimethoxy)phenyl-4-methylene-1,3-dioxolane: II. Preparation and Cationic Polymerization of 2-(x,y,z-Trimethoxyphenyl)-4-methylene-1,3-dioxolane Derivatives 


Vol. 20,  No. 10, pp. 1195-1199, Oct.  1999


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  Abstract

2-(2,4,5-Trimethoxyphenyl)-4-methylene-1,3-dioxolane (1b), 2-(2,4,6-trimethoxyphenyl)-4-methylene-1,3-di-oxolane (2b), and 2-(3,4,5-trimethoxyphenyl)-4-methylene-1,3-dioxolane (3b) were prepared and polymerized with boron trifluoride. Boron trifluoride catalyzed reaction proceeded via mainly ring-opening polymerization and cyclization reaction to yield poly(keto ether) and 3(2H)-dihydrofuranone. The yields of polymer and cyclized product exhibited a dependency on the position of the methoxy substituents in the benzene ring of 2-phenyl-4-methylene-1,3-dioxolane derivatives. Electrophilic attack of methylene or oxygen atom on 4-meth-ylene-1,3-dioxolane ring were suggested for the polymerization and cyclization.

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  Cite this article

[IEEE Style]

W. Jang and M. Gong, "2-(Multimethoxy)phenyl-4-methylene-1,3-dioxolane: II. Preparation and Cationic Polymerization of 2-(x,y,z-Trimethoxyphenyl)-4-methylene-1,3-dioxolane Derivatives," Bulletin of the Korean Chemical Society, vol. 20, no. 10, pp. 1195-1199, 1999. DOI: .

[ACM Style]

Won-Cheoul Jang and Myoung-Seon Gong. 1999. 2-(Multimethoxy)phenyl-4-methylene-1,3-dioxolane: II. Preparation and Cationic Polymerization of 2-(x,y,z-Trimethoxyphenyl)-4-methylene-1,3-dioxolane Derivatives. Bulletin of the Korean Chemical Society, 20, 10, (1999), 1195-1199. DOI: .