HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405657Generated: October 25, 2026
Azobisisobutyronitrile → MAU 2-(N,N-dimethylamino)ethyl acrylate
https://huagongshe.com/reaction/405657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 2-(Dimethylamino)ethyl acrylate | HCID 17111 | — |
| Reactant | 11-(Methacryloylamino)undecanoic acid | HCID 2764185 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | MAU 2-(N,N-dimethylamino)ethyl acrylate | HCID 131731616 | 162.4% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08753686B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-37264b3a59d0413da954ad40b551bd50 |
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| Source note | uspto-grants-2014_06 |
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