HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Disodium → (24R)-5,7-cholestadiene-3beta,24,25-triol 3-tetrahydropyranyl ether
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Disodium | HCID 141233 | — |
| Edukt | (24R)-22xi-phenylsulfonyl-5,7-cholestadiene-3beta,24,25-triol 3-tetrahydropyranyl ether | HCID 70546883 | — |
| Katalysator | Sodium amalgam | HCID 9837419 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (24R)-5,7-cholestadiene-3beta,24,25-triol 3-tetrahydropyranyl ether | HCID 22821223 | 93% |
Reaktionsschritte
A mixture of 1 g of anhydrous disodium hydrogenephosphate and 3.2 g of 5% sodium-amalgam was added to a solution of 160 mg of (24R)-22ξ-phenylsulfonyl-5,7-cholestadiene-3β,24,25-triol 3-tetrahydropyranyl ether in 5 ml of methanol in an argon stream under stirring, and the mixture was stirred for 30 minutes at room temperature. To the reaction mixture 10 ml of methanol was added and the precipitate was filtered. The filtrate was evaporated under reduced pressure and the residue was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydous sodium sulfate. The solvent was evaporated under reduced pressure to give 11.6 mg (93%) of (24R)-5,7-cholestadiene-3β,24,25-triol 3-tetrahydropyranyl ether.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04344888 |
| Quelldatensatz | uspto-grants-1982_08 |
| ORD ID | ord-8dc725055a3c48629a0baad1201e99fe |
| Quellennotiz | uspto-grants-1982_08 |