HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 463532Erstellt: 23. Oktober 2026
Deoxycholic Acid → 12alpha-Hydroxy-3-oxo-5beta-cholan-24-oic Acid
https://huagongshe.com/de/reaction/463532
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Deoxycholic Acid | HCID 222528 | — |
| Lösungsmittel | Chloroform ethanol | HCID 21889567 | — |
| Produkt | 12alpha-Hydroxy-3-oxo-5beta-cholan-24-oic Acid | HCID 160738 | 25,9% |
Reaktionsschritte
The above mixture of oxidation products of deoxycholic acid (310 mg) resulted from the eluate of chloroform-ethanol (97:3, v/v) was dissolved in a small amount of chloroform-ethanol (99:1, v/v) and the solution was absorbed on silica gel (20 g) column. The column was eluted with chloroform-ethanol (98:2, v/v) and then with chloroform-ethanol (97:3, v/v). Each 10 ml portions of the eluate was collected in a fraction tube. Fractions which showed a corresponding single spot by thin layer chromatography were combined and the solvent was distilled off by a rotary evaporator. As the results, 12α-hydroxy-3-keto-5β-cholanic acid (80 mg) was obtained from the first half of the fractions eluted with chloroform-ethanol (98:2, v/v) and 12α-hydroxy-3-keto-4-cholenic acid (10 mg) was obtained from the latter half thereof. 12α-Hydroxy-3-keto-5β-pregnan-20α-carboxylic acid (5 mg) was obtained from the first half of the fractions eluted with chloroform-ethanol (97:3, v/v) and 12α-hydroxy-3-keto-chola-1,4 -dienic acid (10 mg) was obtained from the latter half thereof.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04520102 |
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| Quelldatensatz | uspto-grants-1985_05 |
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| ORD ID | ord-69030becfde94377ac2b52cf29dee9fe |
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| Quellennotiz | uspto-grants-1985_05 |
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