Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Oxygen | HCID 977 | — |
| Edukt | Methyl Acrylate | HCID 7294 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 3,4-Dimethoxyphenyl methyl ketone | HCID 14328 | — |
| Edukt | HCID 178506586 | HCID 178506586 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | HCID 19369950 | HCID 19369950 | — |
Reaktionsschritte
100 ml of a 0.1 M solution of samarium(II) iodide in tetrahydrofuran is mixed, with oxygen carefully excluded, with the solution of 710 mg of 3,4-dimethoxyacetophenone, 500 mg of methyl acrylate and 350 mg of tert-butanol in 5 ml of tetrahydrofuran. The reaction solution is mixed thoroughly, allowed to stand for two hours at room temperature and then poured into 100 ml of 20% hydrochloric acid. It is stirred for two hours at room temperature and extracted with diethyl ether. The ether phase is washed with sodium thiosulfate solution and water, dried on sodium sulfate and concentrated by evaporation in a vacuum. The oily residue is chromatographed on a silica gel column (Kromasil 100/10 μm) with a hexane-tert-butyl methyl ether mixture (4:1). 570 mg of (R,S)-5-(3,4-dimethoxyphenyl)-5-methyl-dihydro-2-furanone is eluted, melting point 71.2° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06011060 |
|---|
| Quelldatensatz | uspto-grants-2000_01 |
|---|
| ORD ID | ord-2f2a8f24c2ce48d2844e84f48e2d08ed |
|---|
| Quellennotiz | uspto-grants-2000_01 |
|---|