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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242760생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/242760

반응식

참여 물질

역할이름HCID투입량
반응물Vinyl etherHCID 8024—
반응물2,5-Furandione, polymer with 1-tetradeceneHCID 161711—
반응물2,5-Furandione, polymer with 1-octadeceneHCID 168344—
반응물Maleic anhydride deceneHCID 22121024—
생성물Furan-2,5-dione--methoxyethene (1/1)HCID 62708—
생성물Maleic anhydride octadecyl vinyletherHCID 86676835—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653190B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-e770e9797cfc48beadc854efe1f1af8c
출처 메모uspto-grants-2014_02