HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Furan → 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Furan | HCID 8029 | — |
| Edukt | Acetic acid, 2,2-dichloro-, 1,1'-anhydride | HCID 77772 | — |
| Edukt | 6-Methoxycarbonyl-1-carboxy-3-hexyne | HCID 10976151 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne | HCID 11020812 | 65% |
Reaktionsschritte
A mixture of 6-methoxycarbonyl-1-carboxy-3-hexyne [VI-1] (18.4 g, 0.1 mole), furan (13.6 g, 0.2 mole), dichloroacetic anhydride (28.8 g, 0.12 mole), boron trifluoride ether complex (3.2 g) and toluene (100 ml) is reacted at 20°-30° C. for 10 hours. After completion of the reaction, the reaction mixture is cooled, and washed successively with water, 5% aqueous sodium carbonate solution and water, and the organic layer is dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography to give 1-oxo-1-furyl-7-methoxycarbonyl-4-heptyne [VII-1] (15.2 g, yield; 65%), b.p. 120°-125° C./0.3 mmHg.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05191109 |
| Quelldatensatz | uspto-grants-1993_03 |
| ORD ID | ord-8629c017070743739acd5e75fd93c1ef |
| Quellennotiz | uspto-grants-1993_03 |