HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydroquinone → (+/-)-trans-1,2-DI methoxy-4-(2-nitrocyclohex-4-enyl)benzene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydroquinone | HCID 785 | — |
| Edukt | 1,3-Butadiene | HCID 7845 | — |
| Edukt | 1,2-Dimethoxy-4-(2-nitrovinyl)benzene | HCID 709688 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | (+/-)-trans-1,2-DI methoxy-4-(2-nitrocyclohex-4-enyl)benzene | HCID 53874256 | 76,3% |
Reaktionsbedingungen
| Temperatur | 160 °C |
|---|
Reaktionsschritte
50.0 g of 3,4-dimethoxy-ω-nitrostyrene and 1.0 g (9.1 mmol) of hydroquinone are suspended in 200 ml of abs. toluene and treated at -70° C. with 55.0 g (1.02 mol) of liquid 1,3-butadiene. The mixture is stirred at 160° C. for 6 days in an autoclave and then cooled. Some of the solvent is distilled off in vacuo, and the resulting precipitate is filtered off with suction and recrystallized in ethanol. M.p.: 113.5-115.5° C.; yield 76.3% of theory.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06127378 |
| Quelldatensatz | uspto-grants-2000_10 |
| ORD ID | ord-80b19b11bbcd4405bbfa02d15544a6ef |
| Quellennotiz | uspto-grants-2000_10 |