HuagongsheHuagongshe Chemistry Print Report · For research reference only
Styrene → 1-Chloro-4-(2-phenylethenyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Product | 1-Chloro-4-(2-phenylethenyl)benzene | HCID 95304 | 43.3% |
Reaction Steps
The procedure described in Example 1 is followed, except that 17.5 g (0.1 mol) of 4-chlorobenzoyl chloride, 13.02 g (0.125 mol) of styrene, 35.37 g (0.1 mol) of tri-2-ethylhexylamine and 0.1773 g (0.01 mol) of palladium chloride are used. After a reaction time of 4 hours at 120° C., 9.3 g (0.0433 mol) of 4-chlorostilbene, corresponding to a yield of 43.3% of theory, are obtained in the form of white flakes; melting point 129°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04335055 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-f7676bf82f5f4da09f399f07b190833e |
| Source note | uspto-grants-1982_06 |