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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 405657생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물2-(Dimethylamino)ethyl acrylateHCID 17111—
반응물11-(Methacryloylamino)undecanoic acidHCID 2764185—
용매MethanolHCID 887—
생성물MAU 2-(N,N-dimethylamino)ethyl acrylateHCID 131731616162.4%

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08753686B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-37264b3a59d0413da954ad40b551bd50
출처 메모uspto-grants-2014_06