HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Styrene → trans-Stilbene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Styrene | HCID 7501 | — |
| Edukt | 3-Bromoquinoline | HCID 21413 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Katalysator | Tetraphenylphosphonium Chloride | HCID 164911 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1,1-Diphenylethylene | HCID 10740 | 14,1% |
| Produkt | 3-Bromoquinoline | HCID 21413 | — |
| Produkt | trans-Stilbene | HCID 638088 | 85,1% |
| Produkt | cis-Stilbene | HCID 5356785 | 0,8% |
Reaktionsschritte
A reaction is performed as described in Example 1, except that 3.9 mg (0.015 mmol) of (CH2CN)2PdCl2, 34.9 mg (0.09 mmol) of Ph4PCl, 496.0 mg (6.05 mmol) of anhydrous sodium acetate, 638.74 mg (3.07 mmol) of 3-bromoquinoline and 427.0 mg (4.1 mmol) of styrene are reacted in 1.5 ml of DMF. Stirring is performed at 130° C. for 5 hours. According to the processing described in Example 1, a 72.5% yield of Heck products (85.1% trans-stilbene, 0.8% cis-stilbene, and 14.1% 1,1-diphenylethene) is obtained with 78.5% conversion of 3-bromoquinoline.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06316675B1 |
| Quelldatensatz | uspto-grants-2001_11 |
| ORD ID | ord-dd08380619e74406b89f84d676a720ba |
| Quellennotiz | uspto-grants-2001_11 |