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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405662Generated: October 30, 2026

Azobisisobutyronitrile → HCID 131731622, compound

https://huagongshe.com/reaction/405662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantSodium HydroxideHCID 14798—
Reactant2-(Methacryloyloxy)ethyl dihydrogen phosphateHCID 90551—
Reactant11-(Methacryloylamino)undecanoic acidHCID 2764185—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 131731622HCID 13173162255.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

In a mixed solvent of 75 g of methanol and 25 g of ion-exchanged water were dissolved 18.40 g (68.32 mmol) of 11-methacrylamidoundecanoic acid (MAU), 1.60 g (7.59 mmol) of 2-methacryloxyethyl phosphoric acid (Phosmer-M: Uni-Chemical Co.), 0.30 g (7.59 mmol) of sodium hydroxide, and 0.31 g (1.89 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, a gelatinous product was obtained. This product was dried under reduced pressure, and 6.0 g of the dried material was added to 200 g of methanol. After sufficient stirring, insoluble material was removed by filtration. The obtained solution was dropwise added into a large excess of ethyl acetate, and the resulting precipitate was collected by filtration under suction. After drying under reduced pressure, 2.01 g of random MAU/2-methacryloxyethyl phosphoric acid copolymer (90/10) was obtained. The weight average molecular weight was 190000.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08753686B2
Source datasetuspto-grants-2014_06
ORD IDord-939768e41d7c4e51b0574b06167fca0b
Source noteuspto-grants-2014_06