HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 255945Erstellt: 25. Oktober 2026
2-Methylbenzenesulfonic acid → N-[(2-phthalimidoethoxy)methyl]acrylamide
https://huagongshe.com/reaction/255945
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| Edukt | 4-Methoxyphenol | HCID 9015 | — |
| Edukt | N-Methylolacrylamide | HCID 13543 | — |
| Edukt | Hydroxyethylphthalimide | HCID 21422946 | — |
| Edukt | Isobornylmethacrylate | HCID 71311141 | — |
| Lösungsmittel | Acrylonitrile | HCID 7855 | — |
| Produkt | N-[(2-phthalimidoethoxy)methyl]acrylamide | HCID 13587414 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04699965 |
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| Quelldatensatz | uspto-grants-1987_10 |
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| ORD ID | ord-97b66427b0634bcbac763d5a84bd825d |
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| Quellennotiz | uspto-grants-1987_10 |
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