Alanine-methacrylamide → HCID 178449942, Verbindung
Reaktionsgleichung
Cl.[C:2]([NH2:7])(=[O:6])[C:3]([CH3:5])=[CH2:4].[NH2:8][C@H:9]([C:17]([OH:19])=[O:18])[CH2:10][CH2:11][CH2:12][NH:13][C:14](=[NH:16])[NH2:15].[C:20]([NH2:25])(=[O:24])[C:21]([CH3:23])=[CH2:22].N[C@H](C(O)=O)C>O>[C:2]([NH2:7])(=[O:6])[C:3]([CH3:5])=[CH2:4].[NH2:8][C@H:9]([C:17]([OH:19])=[O:18])[CH3:10].[C:20]([NH2:25])(=[O:24])[C:21]([CH3:23])=[CH2:22].[NH2:8][C@H:9]([C:17]([OH:19])=[O:18])[CH2:10][CH2:11][CH2:12][NH:13][C:14](=[NH:15])[NH2:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Arginine-methacrylamide hydrochloride(10.53 g) and 13.90 g of the aforementioned alanine-methacrylamide were dissolved in 100 ml of distilled water, and bubbled with nitrogen gas for 1 hour. Potassium persulfate(250 mg) was added to the solution, and dissolved in it. The reaction mixture was refluxed by heating for 3 hours, then cooled to room temperature, and poured into acetone, so that precipitates were deposited. The supernatant was discarded, and acetone was again added to the precipitates and obtained mixture was stirred. The deposition was collected by filtration and dried to obtain the target polymer (white powder, 20.90 g).
Aufarbeitung
- custombubbled with nitrogen gas for 1 hour
- additionPotassium persulfate(250 mg) was added to the solution
- dissolutiondissolved in it
- temperatureThe reaction mixture was refluxed
- temperatureby heating for 3 hours
- additionpoured into acetone
- customso that precipitates
- additionacetone was again added to the
- customprecipitates
- customobtained mixture
- filtrationThe deposition was collected by filtration
- customdried
- customto obtain the target polymer (white powder, 20.90 g)
Quellen und Nachweise
- ORD-Eintrag
- ord-2dbb898dd13a4e53b69224bbf57f53a4
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06703468B1
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