HuagongsheHuagongshe Chemistry Print Report · For research reference only
Styrene → 1,4-Diphenyl-1,3-butadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Benzene, (3-chloro-1-propenyl)- | HCID 94242 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1,4-Diphenyl-1,3-butadiene | HCID 13452 | 27.7% |
Reaction Steps
The procedure described in Example 1 is followed, except that 16.7 g (0.1 mol) of cinnamyl chloride, 13.0 g (0.125 mol) of styrene, 23.3 g (0.125 mol) of tri-n-butylamine, 100 ml of chlorobenzene and 0.225 g (0.001 mol) of palladium acetate are used. After a reaction time of 5 hours at a bath temperature of 140° C., 5.7 g (0.0277 mol) of 1,4-diphenyl-1,3-butadiene, corresponding to a yield of 27.7% of theory, are obtained; melting point 150°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04335055 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-cae6ce65874942e6b61ce420fb9fd0a9 |
| Source note | uspto-grants-1982_06 |