HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620694Generated: October 29, 2026
Azobisisobutyronitrile → HCID 86742238, compound
https://huagongshe.com/reaction/620694
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Methacrylonitrile | HCID 31368 | — |
| Reactant | 2,2,2-Trifluoro-1-phenylethyl 2-chloroprop-2-enoate | HCID 14534567 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 86742238 | HCID 86742238 | — |
Reaction Steps
1.26 g of 1-phenyl-2,2,2-trifluoroethyl α-chloroacrylate, 0.74 g of methacrylnitrile, 0.52 ml of a benzene solution containing 0.1 wt% of azobisisobutyronitrile and 1.75 ml of benzene were introduced into a flask, and the flask was evacuated by vacuuming in a usual manner. The mixture in the flask was stirred at 70° C. for 20 hours, and then the reaction product was poured into methanol. The polymer was permitted to precipitate, then subjected to filtration and dried to obtain a 1-phenyl-2,2,2-trifluoroethyl α-chloroacrylate/methacrylnitrile copolymer. The copolymerization ratio was found to be 50/50 by molar ratio as a result of the elemental analysis. The weight average molecular weight was found to be 4.0×105 as calculated as polystyrene, as a result of the GPC measurement.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822721 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-7618a283676f4dc6abfe8b1019a07fdc |
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| Source note | uspto-grants-1989_04 |
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