HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Iodine → 2,3,4,5-Tetrahydro-alpha-methyl-1-benzoxepine-8-methanol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 8-Bromo-2,3,4,5-tetrahydrobenzo[b]oxepine | HCID 19935534 | — |
| Katalysator | 1,2-Dibromoethane | HCID 7839 | — |
| Produkt | 2,3,4,5-Tetrahydro-alpha-methyl-1-benzoxepine-8-methanol | HCID 19935427 | — |
Reaktionsbedingungen
| Temperatur | -10 °C |
|---|
Reaktionsschritte
7.3 g of 8-bromo-2,3,4,5-tetrahydro-1-benzoxepine in 30 ml of absolute tetrahydrofuran were added under argon to 930 mg shavings and a granule of iodine. The reaction was intitiated by the addition of a few drops of 1,2-dibromoethane and has finished after 2 hours. Thereafter, the reaction mixture was cooled to -10° C. and excess acetaldehyde was distilled into the reaction vessel. After 10 minutes, the mixture was hydrolyzed with saturated sodium bicarbonate (NaHCO3) solution, extracted with ether, washed with water, dried and evaporated to dryness. Chromatography on silica gel (petroleum ether/ethyl acetate 3:1) yielded 4.93 g of 2,3,4,5-tetrahydro-α-methyl-1-benzoxepine-8-methanol as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05164387 |
| Quelldatensatz | uspto-grants-1992_11 |
| ORD ID | ord-c8c67de915d2404f9289478b5992c195 |
| Quellennotiz | uspto-grants-1992_11 |