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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28072Generated: October 25, 2026

Ethylene → Ethylene/Ethyl Acrylate Allyl Acrylate Maleic Anhydride

https://huagongshe.com/reaction/28072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyleneHCID 6325—
ReactantBoron trifluorideHCID 6356—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
ReactantEthyl AcrylateHCID 8821—
ReactantAllyl acrylateHCID 13835—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
ProductEthylene/Ethyl Acrylate Allyl Acrylate Maleic AnhydrideHCID 86737232—

Reaction Steps

A 7.57-liter stirred autoclave was charged under nitrogen with 4000 ml. of methylene chloride, 400 grams of ethyl acrylate, 20 grams of maleic anhydride, 1.2 grams of allyl acrylate, and 1.0 gram of azobis(isobutyronitrile). It was then sealed, charged with 300 grams of boron trifluoride, and pressured to 21 kg./sq. cm. with ethylene. The subsequent copolymerization at 25° C. was continued until pressure measurement indicated that ethylene uptake had ceased (about two hours later). The reaction was quenched by addition of one liter of diethyl ether. Volatiles were removed by steam-stripping in a well-ventilated hood. The terpolymer thereby obtained was dissolved in acetone, precipitated in water in a blender, and oven-dried. Yield: 415 grams.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225476
Source datasetuspto-grants-1980_09
ORD IDord-64a9bf2ab9ad4033bab0329dec4fa910
Source noteuspto-grants-1980_09