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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736580Generated: October 25, 2026

Azobisisobutyronitrile → Norbornene methyl methacrylate

https://huagongshe.com/reaction/736580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMethyl MethacrylateHCID 6658—
Reactant2-NorborneneHCID 10352—
ReactantEthylaluminum sesquichlorideHCID 25508—
ReactantHydrochloride methanolHCID 21893726—
SolventTolueneHCID 1140—
ProductNorbornene methyl methacrylateHCID 86604938—

Reaction Steps

Norbornene (8.8 g, 93 mmol), methyl methacrylate (5 mL, 47 mmol), and AIBN (0.23 g, 1.40 mmol) were charged into a 250 mL Schlenk flask and dissolved in 30 mL of toluene. Ethylaluminum sesquichloride (12.7 g, 51.4 mmol) was charged into a 100 mL flask and dissolved in 20 mL of toluene. The toluene solution of ethylaluminum sesquichloride was slowly dropped to the 250 mL Schlenk flask at −70° C. The reaction temperature was raised to room temperature while stirring the mixture for 2 hours, and then the reaction was performed at 65° C. for 12 hours. The reaction solution turned to light green in color during the reaction. After the reaction was completed, the reaction solution was slowly dropped to 3000 cc of 5% v/v HCl—MeOH to precipitate a white polymer, which was filtered through a glass filter and dried in a vacuum oven at 70° C. for 12 hours to obtain a norbornene-methyl methacrylate copolymer (0.3 g: 3.0% by weight based on the total weight of used monomers). The copolymer had a Tg of 167° C., a molecular weight (Mw) of 10,700, and Mw/Mn of 3.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595369B2
Source datasetuspto-grants-2009_09
ORD IDord-95d961234c0640db929e4f5691aae3d3
Source noteuspto-grants-2009_09