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HRID 323661作成日:2026年10月25日

p-(Trifluoromethoxy)phenyl isocyanate → 3,5-dichloro-4-(2-(N'-(4-trifluoromethoxyphenyl)ureido)ethoxy)-1-(3,3-dichloro-2-propenyloxy)benzene

https://huagongshe.com/reaction/323661

反応式

関与物質

役割名称HCID仕込み量
反応物p-(Trifluoromethoxy)phenyl isocyanateHCID 92298—
反応物3,5-Dichloro-4-(2-aminoethoxy)-1-(3,3-dichloro-2-propenyloxy)benzeneHCID 22006752—
溶媒TolueneHCID 1140—
生成物3,5-dichloro-4-(2-(N'-(4-trifluoromethoxyphenyl)ureido)ethoxy)-1-(3,3-dichloro-2-propenyloxy)benzeneHCID 2200673546.5%

反応手順

A solution of 0.20 g of 3,5-dichloro-4-(2-aminoethoxy)-1-(3,3-dichloro-2-propenyloxy)benzene and 0.14 g of 4-trifluoromethoxyphenyl isocyanate dissolved in 10 ml of toluene was heated under reflux, while stirring, for 12 hours, and the reaction mixture was then concentrated to give a residue. The residue was subjected to silica gel chromatography, which afforded 0.15 g of 3,5-dichloro-4-(2-(N′-(4-trifluoromethoxyphenyl)ureido)ethoxy)-1-(3,3-dichloro-2-propenyloxy)benzene (46% yield), m.p., 1 25.4° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06214835B1
出典データセットuspto-grants-2001_04
ORD IDord-6ee44e81fb23411ebd4033320cd1981d
出典メモuspto-grants-2001_04