Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 1-Pentanol | HCID 6276 | — |
| Edukt | 2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)acetic acid | HCID 319935 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 21880419 | HCID 21880419 | 643,8% |
Reaktionsschritte
In a separable flask equipped with a Dean-Stark trap, maleimidoacetic acid (reagent grade) (31.0 g, 0.2 mol), p-toluenesulfonic acid (reagent grade) (5.2 g, 0.03 mol), and toluene (reagent grade) (300 ml) were charged. Then, the mixture was stirred and reacted under reduced pressure at 80° C. for 1 hour with dropwise addition of n-pentanol (reagent grade) (17.6 g, 0.2 mol). After the dropwise addition, the mixture was stirred for another 4 hours for allowing the reaction to be continued. During the reaction, the water formed was removed with the Dean-Stark trap. After the reaction, toluene (300 ml) was added and the mixture was washed three times with ion-exchanged water (100 ml). Then, the organic phase obtained was collected and subjected to removal of the toluene by evaporation using an evaporator and a vacuum dryer to give n-pentyl maleimidoacetate (43.5 g). (Yield: ca. 91%. The absence of maleimidoacetic acid and n-pentanol was verified by GPC measurement. The presence of n-pentyl maleimidoacetate was verified by 1H-NMR measurement using DMSO-d6. This compound is referred to hereinafter as Compound A1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754178B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-ac19d27a89eb4590b6786fc66fe0f6b2 |
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| Quellennotiz | uspto-grants-2014_06 |
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