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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242760Generated: October 26, 2026

Vinyl ether → Furan-2,5-dione--methoxyethene (1/1)

https://huagongshe.com/reaction/242760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl etherHCID 8024—
Reactant2,5-Furandione, polymer with 1-tetradeceneHCID 161711—
Reactant2,5-Furandione, polymer with 1-octadeceneHCID 168344—
ReactantMaleic anhydride deceneHCID 22121024—
ProductFuran-2,5-dione--methoxyethene (1/1)HCID 62708—
ProductMaleic anhydride octadecyl vinyletherHCID 86676835—

Reaction Steps

The cyclic carboxylic anhydride can be used in an amount of about 10-70, preferably about 35-70 mol percent. More preferably 45-60 mol percent of ethylenically unsaturated cyclic anhydride is copolymerized with 40-55 mol percent of at least one C2 to C30 aliphatic 1-alkene to produce a copolymer such as, e.g., a maleic anhydride/octadecene copolymer, maleic anhydride/decene copolymer, and maleic anhydride/tetradecene copolymer. It is also contemplated to copolymerize 45-60 mol percent of a cyclic carboxylic anhydride with 40-50 mol percent of a vinylether of preferably less than 30 carbon atoms to produce a copolymer such as, e.g. a maleic anhydride/octadecyl vinylether copolymer or maleic anhydride/methylvinylether copolymer. It is further contemplated to copolymerize 45-60 mole percent of a cyclic carboxylic anhydride with 40-55 mol percent styrene to produce, e.g. a maleic anhydride/styrene copolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653190B2
Source datasetuspto-grants-2014_02
ORD IDord-e770e9797cfc48beadc854efe1f1af8c
Source noteuspto-grants-2014_02