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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 405657Erstellt: 23. Oktober 2026

Azobisisobutyronitrile → MAU 2-(N,N-dimethylamino)ethyl acrylate

https://huagongshe.com/de/reaction/405657

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
Edukt2-(Dimethylamino)ethyl acrylateHCID 17111—
Edukt11-(Methacryloylamino)undecanoic acidHCID 2764185—
LösungsmittelMethanolHCID 887—
ProduktMAU 2-(N,N-dimethylamino)ethyl acrylateHCID 131731616162,4%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

In 59.68 g of methanol were dissolved 18.88 g (70.12 mmol) of 11-methacrylamidoundecanoic acid (MAU), 1.12 g (7.79 mmol) of 2-(N,N-dimethylamino)ethyl acrylate (Tokyo Chemical industry Co.), and 0.32 g (1.95 mmol) of azobisisobutyronitrile (Nacalai Tesque, Inc.). The solution was deaerated by bubbling nitrogen for 60 minutes. The container was covered with a septum, and the polymerization was conducted by heating at 60° C. for 20 hours. After the completion of the polymerization reaction, the solution was concentrated to dryness under reduced pressure, and the solid was dissolved in 60 g of dimethylformamide. The obtained solution was dropwise added into a large excess of diethyl ether, and the resulting precipitate was collected by filtration under suction. After drying under reduced pressure, 5.22 g of random MAU/2-(N,N-dimethylamino)ethyl acrylate copolymer (90/10) was obtained (yield: 26.1%). The weight average molecular weight was 130000.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08753686B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-37264b3a59d0413da954ad40b551bd50
Quellennotizuspto-grants-2014_06