HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sulfuric Acid → 4-(7,12-Dihydroxy-3-methanesulfonyloxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl) pentanoic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | Cholic Acid | HCID 221493 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 4-(7,12-Dihydroxy-3-methanesulfonyloxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl) pentanoic acid | HCID 18425131 | — |
Reaktionsschritte
100 g of cholic acid are dissolved in 500 ml of pyridine and 23.1 ml of mesyl chloride are added dropwise at 0° C. over a period of 30 minutes. The mixture is stirred at RT for 3 hours, then poured onto a solution of 400 ml of H2SO4 in 3 l of water at 0° C. and extracted 4 times with 750 ml of EA each time. The organic phase is dried over Na2SO4 and the solvent is removed in vacuo. The residue is crystallized using diisopropyl ether and 117.1 g are obtained; m.p. 121° C. (with decomposition). Rf (EA/HEP/acetic acid 5:5:1)=0.31 MS (FAB): 487 (M+H)+
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06166002 |
| Quelldatensatz | uspto-grants-2000_12 |
| ORD ID | ord-4bb7fd5933aa45639c928c5bb31f2603 |
| Quellennotiz | uspto-grants-2000_12 |