HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614682Generated: October 31, 2026
Azobisisobutyronitrile → HCID 19795469, compound
https://huagongshe.com/reaction/1614682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Butyl Acrylate | HCID 8846 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 19772431 | HCID 19772431 | — |
| Product | HCID 19795469 | HCID 19795469 | — |
Reaction Steps
Butyl acrylate (24.4 g, 0.19 mol), and N-(3-(methacrylamido) propyl)-3,4,5-triacetoxybenzamide (IV) (4.20 g, 0.010 mol) were combined with 110 mL ethyl acetate and azobis(isobutyronitrile)(0.16 g) in a vessel sealed with a septum. The vessel was purged with N2 and heated to 60° C. with agitation for 24 h. Additional AIBN (0.16 g) was added and the mixture was heated for an additional 24 h. Yield 124.7 g solution, 22.6% solids. 1H NMR of an evaporated sample showed no residual monomers and was consistent with the desired copolymer structure. Inherent viscosity in ethyl acetate at 25° C., c=0.238 g/dL; ηinh=0.44. The polymer in ethyl acetate solution was then dispersed in a gelatin solution containing surfactant, followed by removal of the ethyl acetate by evaporation before use.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05198517 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-8bb0890b308544c9a8869360a059bb6b |
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| Source note | uspto-grants-1993_03 |
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