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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179098Generated: October 31, 2026

Azobisisobutyronitrile → HCID 131726626, compound

https://huagongshe.com/reaction/1179098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
Reactanttert-Butyl methacrylateHCID 11448—
Reactant3-(Trimethoxysilyl)propyl methacrylateHCID 17318—
ReactantMethyl bicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 250075—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131726626HCID 131726626—

Reaction Steps

To 25 ml of tetrahydrofuran in 100 ml of a round-shaped flask were added 5 g of 3-(trimethoxysilyl)propyl methacrylate, 4 g of t-butyl methacrylate, 3 g of methyl 5-norbornene-2-carboxylate and 3 g of maleic anhydride. Then, 0.13 g of AIBN (azobisisobutyronitrile) as a polymerization initiator was added to the resulting mixture, and reacted at 67° C. under a nitrogen atmosphere for 24 hours. Next, the resulting mixture was cooled at room temperature, and poured into a beaker including 500 ml of ethyl ether to precipitate the resulting mixture. Thereafter, the precipitate was filtered and dehydrated at room temperature, thereby obtaining poly(3-(trimethyoxysilyl)propyl methacrylate/t-butyl methacrylate/methyl 5-norbornene-2-carboxylate/maleic anhydride) having a molecular weight of 1,800 represented by formula 1a (yield: 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279256B2
Source datasetuspto-grants-2007_10
ORD IDord-7a45437b565f4d20b1f5ced06ecb9bf2
Source noteuspto-grants-2007_10