HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 4-Vinylpyridine styrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 2-Vinylpyridine | HCID 7521 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Vinylpyridine styrene | HCID 12666455 | 20% |
Reaction Steps
In a 200 ml three necked flask were charged 21 g of 4-vinylpyridine, 21 g of styrene and 0.1 g of azobisisobutyronitrile and 90 ml of benzene. The mixture was polymerized at 80° C. for 6 hrs under a nitrogen atmosphere. The reaction liquid was poured into a large amount of n-hexane to thereby obtain white precipitates. After filtering and drying, a white powder was obtained. The molar fraction of vinylpyridine in the polymer was 0.57 and the yield was 20%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04245027 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-2fc78f28946d42f0a1e6089859ad9551 |
| Source note | uspto-grants-1981_01 |