HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dicyclopropyl ketone → 4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dicyclopropyl ketone | HCID 70721 | — |
| Edukt | Cyclopropanecarboxylic acid, 1-benzoyl-2-ethenyl-, ethyl ester | HCID 11053884 | — |
| Edukt | Tricaprylylmethyl ammonium chloride | HCID 77620884 | — |
| Produkt | 4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran | HCID 20191550 | — |
Reaktionsschritte
4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran was obtained in the usual manner by isomerizing ethyl 2-vinyl-1-benzoylcyclopropane-1-carboxylate. To catalyze the isomerization, tricaprylylmethylammonium chloride was employed at a 20 percent weight level. The mixture was heated at 150° C. for about two hours after which time only about 7 percent of the cyclopropyl ketone remained. After two distillations of the resulting isomerized product, essentially pure 4-carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran was obtained (B.P. 110° C. @ 0.1 mm Hg; nD25° 1.5570). The product had a pleasing aroma that was somewhat coumarin-like in odor character.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04515978 |
| Quelldatensatz | uspto-grants-1985_05 |
| ORD ID | ord-7f5549cea3aa4973ba7b9d0921684422 |
| Quellennotiz | uspto-grants-1985_05 |