HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3beta, 5alpha,25-Tri-hydroxy-cholestane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3beta-Acetoxy-5alpha,25-dihydroxy cholestane | HCID 20739547 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3beta, 5alpha,25-Tri-hydroxy-cholestane | HCID 54528626 | — |
Reaction Steps
A solution of 3β-acetoxy-5α,25-dihydroxy-cholestane (IV) in 40 cc of methanol and 10 cc of dioxane was treated with 6 cc of a 10% solution of sodium hydroxide and refluxed for 3 hours. The reaction mixture was neutralized with a solution of 5% aqueous hydrochloric acid, extracted with ether and washed with water. The ether solution was evaporated in vacuo and the residue was recrystallized from ether to give 850 mg of the 3β, 5α,25-tri-hydroxy-cholestane (VI) m.p. 202°-204° Nmr δ 0.67 (s, 3H), 0.9 (d, J=5 cps, 3H), 1.22 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03963765 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-f1df168a7ff341b6b33e359bb3ef9838 |
| Source note | uspto-grants-1976_06 |