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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076454Generated: October 27, 2026

Azobisisobutyronitrile → Methyl methacrylate linoleyl methacrylate methacrylic acid

https://huagongshe.com/reaction/1076454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMethyl MethacrylateHCID 6658—
ReactantMethacryloyl chlorideHCID 13528—
ReactantMethyl linoleateHCID 5284421—
ReactantLinoleyl alcoholHCID 5365682—
ReactantAluminium lithium hydrideHCID 21226445—
SolventBenzeneHCID 241—
ProductMethyl methacrylate linoleyl methacrylate methacrylic acidHCID 86733418—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 90 parts of methyl methacrylate, 10 parts of methacrylyl chloride, and 2 parts of azobisisobutyronitrile was added, over a period of 3 hours, to 250 parts of dry benzene maintained at reflux under a nitrogen atmosphere. The mixture was refluxed for an additional 14 hours, cooled to 20°C and then stirred for 1 hour with 19 parts of linoleyl alcohol, prepared by lithium aluminium hydride reduction of technical methyl linoleate. The mixture was washed with water then evaporated in vacuo to yield a methyl methacrylate/linoleyl methacrylate/methacrylic acid copolymer. 10 parts of the copolymer was dissolved in 20 parts of toluol and then mixed with 100 parts of a commercial silica-alumina coated rutile titania pigment, and dried in vacuo at 50°C. The resultant solid was finely ground, then oxidised by air in a fluidised bed at 50°C for 24 hours to yield a product containing 0.02m. equiv./g of peroxidic species. When incorporated in polyethylene by the method of Example 1, a polyethylene of improved toughness was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957526
Source datasetuspto-grants-1976_05
ORD IDord-75da238e3f634f2a9c3cce95704c38b6
Source noteuspto-grants-1976_05