HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 4-Ethynylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1-Dodecanethiol | HCID 8195 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Ethynylphenol | HCID 32758 | — |
Reaction Steps
In 100 ml of dioxane were dissolved 176 g (1.0 mole) of p-t-butoxystyrene, 4.0 g (0.02 mole) of dodecylmercaptan and 8.2 g (0.05 mole) of azobisisobutyronitrile, and the resulting solution was subjected to reaction for 10 hours while the internal temperature was kept at 75° C., after which the reaction mixture was subjected to several reprecipitation treatments to remove the unreacted monomer, thereby obtaining poly(p-t-butoxystyrene). Subsequently, this poly(p-t-butoxystyrene) was hydrolyzed with an acid to obtain poly(p-hydroxystyrene) having a Mw of 8,900. This resin is referred to hereinafter as Resin A2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05376498 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-0c98136ceb984f3697222feed78203be |
| Source note | uspto-grants-1994_12 |