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HRID 255945作成日:2026年10月27日

2-Methylbenzenesulfonic acid → N-[(2-phthalimidoethoxy)methyl]acrylamide

https://huagongshe.com/reaction/255945

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylbenzenesulfonic acidHCID 6925—
反応物4-MethoxyphenolHCID 9015—
反応物N-MethylolacrylamideHCID 13543—
反応物HydroxyethylphthalimideHCID 21422946—
反応物IsobornylmethacrylateHCID 71311141—
溶媒AcrylonitrileHCID 7855—
生成物N-[(2-phthalimidoethoxy)methyl]acrylamideHCID 13587414—

反応条件

温度120 °C

反応手順

Approximately equimolar amounts of N-(2-hydroxyethyl phthalimide (about 5 molar percent excess) and dried IBMA were mixed together in a reaction flask with 0.5 weight percent toluene sulfonic acid, based on the weight of IBMA, and 200 ppm MEHQ added. The nearly dry blend was stirred and heated using an external oil bath. When the temperature reached 65° C., a rapid reaction ensued and the reaction mixture partially liquified. After a short period of time, the reaction rate (as evidenced by the isobutyl alcohol removal) almost stopped, and the reaction mixture solidified. The reaction mixture was then rapidly heated to about 120° C., and the reaction again proceeded vigorously, going to near quantitative yields in a few more minutes. The product was a clear, low viscosity liquid at 120° C. which solidified at about 65° C. to a waxy, opaque white solid which was found to be readily soluble in acrylonitrile. The product was the 2-hydroxyethyl phthalimide ether of N-(hydroxymethyl) acrylamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04699965
出典データセットuspto-grants-1987_10
ORD IDord-97b66427b0634bcbac763d5a84bd825d
出典メモuspto-grants-1987_10