HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677910Generated: October 31, 2026
Azobisisobutyronitrile → HCID 86636729, compound
https://huagongshe.com/reaction/1677910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Butyl Acrylate | HCID 8846 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86636729 | HCID 86636729 | 94% |
Reaction Steps
Along with 228 mg (0.08 mmol) of poly(1-vinyl-2-pyrrolidone) macroinitiator prepared in Example 67, 3.3 mg (0.02 mmol) of 2,2′-azobis(isobutyronitrile) and 1.04 g (8.1 mmole) of n-butyl acrylate (same as above) were placed into a glove box with the inside air replaced by nitrogen, followed by stirring at 60° C. for 6 hours. After the completion of the reaction, the reaction mixture was dissolved in 5 ml of N,N-dimethylformamide (DMF), and the solution was then poured into 300 ml of hexane which was being stirred. The resulting polymer precipitate was collected by suction filtration and dried to obtain block copolymer of poly(1-vinyl-2-pyrrolidone-b-n-butyl acrylate) (yield 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008414B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-afd1a9b62f7f4a55bfdd7e50e28182e7 |
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| Source note | uspto-grants-2011_08 |
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