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HRID 323674作成日:2026年10月26日

Dimethylformamide → 3,5-Dichloro-4-(3-phthalimidopropyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene

https://huagongshe.com/reaction/323674

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1-[4-(3,3-Dichloroprop-2-enyloxy)-2,6-dichlorophenoxy]-3-bromopropaneHCID 10884069—
反応物Phthalimide potassium saltHCID 24194345—
溶媒WaterHCID 962—
生成物3,5-Dichloro-4-(3-phthalimidopropyloxy)-1-(3,3-dichloro-2-propenyloxy)benzeneHCID 1850457498%

反応手順

A reaction vessel was charged with 4.09 g of 3,5-dichloro-4-(3-bromopropyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene, 2.41 of potassium phthalimide and 30 ml of N,N-dimethylformamide. After stirring at room temperature for 24 hours, the reaction mixture was poured into water and extracted twice with 150 ml of chloroform. The chloroform layers were combined, washed with diluted hydrochloric acid and diluted aqueous sodium hydroxide, dried over anhydrous magnesium sulfate, and then concen- trated, which afforded 4.67 g of crude 3,5-dichloro-4-(3-phthalimidopropyloxy)-1-(3,3-dichloro-2-propenyloxy)benzene (98% yield).

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-c39107044cc144cbb367bd3d3be69f3f
出典メモuspto-grants-2001_04