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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492312Generated: October 31, 2026

Azobisisobutyronitrile → HCID 86748319, compound

https://huagongshe.com/reaction/1492312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantStyreneHCID 7501—
ReactantGlycidyl methacrylateHCID 7837—
ReactantMaleic AnhydrideHCID 7923—
CatalystAzobisisobutyronitrileHCID 6547—
SolventMethanolHCID 887—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 86748319HCID 86748319516.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

A monomer mixture comprising 600 g of styrene (hereinafter referred to as "St") and 70 g of glycidyl methacrylate (hereinafter referred to as "GMA") was dissolved in 1000 g of methyl ethyl ketone (hereinafter referred to as "MEK") in a four -necked flask fitted with a dropping funnel, a nitrogen inlet tube, a thermometer, a condenser and a stirrer and the solution was heated to 70° C. Another monomer mixture comprising 15 g of azobisisobutyronitrile (hereinafter referred to as "AIBN") as the polymerization initiator, 260 g of St, 70 g of maleic anhydride (hereinafter referred to as "MAH") and 280 g of MEK was stepwise dropped thereinto to initiate polymerization. After 10 h, the flask was cooled to room temperature arid the reaction mixture was immediately poured into a large quantity of methanol. The polymer thus precipitated was recovered by decantation, dried under reduced pressure in a vacuum drier axed Finely pulverized to give 870 g of styrene-maleic anhydride glycidyl methacrylate copolymer (3). According to GPC, the copolymer (3) had a number-average molecular weight (in terms of polystyrene ) of 15,000. The infrared absorption spectrum of the copolymer (3) is given in FIG. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05373057
Source datasetuspto-grants-1994_12
ORD IDord-7a3ce8fea563427bbb6f1fc58b26f871
Source noteuspto-grants-1994_12