HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium;tri(butan-2-yl)boranuide → 3beta-Hydroxy-androstane-11,17-dione
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium;tri(butan-2-yl)boranuide | HCID 4304157 | — |
| Edukt | Androstane-3,11,17-trione | HCID 66657133 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 3beta-Hydroxy-androstane-11,17-dione | HCID 21968764 | 99,2% |
Reaktionsbedingungen
| Temperatur | -78 °C |
|---|
Reaktionsschritte
K-SELECTRIDE® (potassium tri-sec-butylborohydride, 98.39 mL, 98.01 mmol, 1M solution in THF) is added to a solution of Compound 1.13 (33.0 g, 109.27 mmol) in THF (330 mL) over 15 minutes under an inert atmosphere at −78 ° C. and is stirred for about 3-4 h at −78 ° C. The reaction mixture is quenched with aqueous NaOH solution (2M, 70 mL). The crude reaction mixture is diluted with ethyl acetate (500 mL) and the organic layer is washed with water (3×75 mL), saturated brine solution (100 mL) and dried over MgSO4 (75 g). The solvent is removed under vacuum to afford 33 g of crude material. The crude product is subjected to acetylation without purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08883770B2 |
| Quelldatensatz | uspto-grants-2014_11 |
| ORD ID | ord-bc71fd852b374fd485a3d579acfd6eb9 |
| Quellennotiz | uspto-grants-2014_11 |