HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
18-Crown-6 → 1-(2-Methoxyethenyl)-4-(octyloxy)benzene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 18-Crown-6 | HCID 28557 | — |
| Edukt | p-(Octyloxy)benzaldehyde | HCID 90358 | — |
| Edukt | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 1-(2-Methoxyethenyl)-4-(octyloxy)benzene | HCID 53775512 | — |
Reaktionsschritte
Potassium t-butoxide (1.9 g) is added to a slurry of methoxymethyl triphenylphosphonium chloride (6.17 g) and 18-Crown-6 (100 mg) in dry THF (40 ml). The mixture is stirred for 5 min, cooled to 15°, and a solution of 4-octyloxybenzaldehyde (3.52 g) in THF (5 ml) is added dropwise. The reaction mixture is stirred at room temperature for 20 min, diluted with 250 ml hexane, and the resulting mixture filtered through a pad of diatomaceous earth. Evaporation of the filtrate leaves crude 1-(2-methoxyethenyl)-4-(octyloxy)benzene as a mixture of cis and trans isomers, containing about 15 mol % triphenylphosphine oxide. The crude material may be used as is, or may be chromatographed with 1:1 hexanedichloromethane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05464865 |
| Quelldatensatz | uspto-grants-1995_11 |
| ORD ID | ord-342bcfb170dd446095d890ba2b2078d3 |
| Quellennotiz | uspto-grants-1995_11 |