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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | Methyl linoleate | HCID 5284421 | — |
| Reactant | Linoleyl alcohol | HCID 5365682 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl methacrylate linoleyl methacrylate methacrylic acid | HCID 86733418 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03957526 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-75da238e3f634f2a9c3cce95704c38b6 |
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| Source note | uspto-grants-1976_05 |
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