HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → Styrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Styrene | HCID 7501 | — |
| Product | 4-Vinylphenol | HCID 62453 | — |
Reaction Steps
300 g of p-t-butoxystyrene, 30 g of styrene, and 1.6 g of azobis-iso-butylonitrile were dissolved in 330 g of dioxane, and reacted for 12 hours under a nitrogen atmosphere at 70° C. After the reaction, unreacted monomers were removed to obtain a copolymer of p-hydroxystyrene and styrene. This resin was hydrolyzed with an acid to produce 180 g of a copolymer of p-hydroxystyrene and styrene with Mw of 18,000. NMR measurement confirmed that the molar ratio of p-hydroxystyrene and styrene was 85:15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05629135 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-7d6daa605c624221bfe40cfaec067b45 |
| Source note | uspto-grants-1997_05 |