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HRID 405657作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物2-(Dimethylamino)ethyl acrylateHCID 17111—
反応物11-(Methacryloylamino)undecanoic acidHCID 2764185—
溶媒MethanolHCID 887—
生成物MAU 2-(N,N-dimethylamino)ethyl acrylateHCID 131731616162.4%

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08753686B2
出典データセットuspto-grants-2014_06
ORD IDord-37264b3a59d0413da954ad40b551bd50
出典メモuspto-grants-2014_06