HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10575424, compound → HCID 86758554, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10575424 | HCID 10575424 | — |
| Reactant | HCID 86758555 | HCID 86758555 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86758554 | HCID 86758554 | 84% |
Reaction Steps
12.5 mL of Jones reagent (33.3 mmol Cr(VI)) are dropped into a solution of 17.8 g of (3β,5β,12α)-3-azido-12-hydroxycholan-24-oic acid methyl ester (41.1 mmol) (prepared analogously to the method described for (3β,5β,7α,12α)-3-azido-7,12-dihydroxycholan-24-oic acid methyl ester in WO-A-95/32741: example 5) in acetone (600 mL) in 90 min at room temperature. After 20 h the mixture is filtered and the solution is evaporated. The residue is dissolved in CHCl3 (400 mL) and the solution is washed with a NaHCO3 saturated aqueous solution then with H2O. The solution is dried and evaporated to give a crude which is crystallized from 96% EtOH to obtain 14.1 g of the desired product (32.9 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06461588B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-f1eaf6f3b72441ff9e7add79c0db7590 |
| Source note | uspto-grants-2002_10 |