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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485502Generated: October 29, 2026

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

https://huagongshe.com/reaction/485502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzenesulfonic acidHCID 6925—
Reactant4-MethoxyphenolHCID 9015—
ReactantN-MethylolacrylamideHCID 13543—
ReactantHydroxyethylphthalimideHCID 21422946—
ReactantIsobornylmethacrylateHCID 71311141—
SolventAcrylonitrileHCID 7855—
ProductN-[(2-phthalimidoethoxy)methyl]acrylamideHCID 13587414—

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536582
Source datasetuspto-grants-1985_08
ORD IDord-9e4f2b49e01748029cadbd2e11975579
Source noteuspto-grants-1985_08