HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(Cholest-5-en-3beta-yloxy)-1-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Cholesteryl tosylate | HCID 10907651 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(Cholest-5-en-3beta-yloxy)-1-ethanol | HCID 14187335 | 70.3% |
Reaction Steps
A solution of 10 g of cholesterol tosylate and 25.3 g of ethylene glycol in 180 ml of dioxan is heated to 120° C. while stirring. The mixture is then treated with 200 ml of water and extracted with ether. The ethereal phase is washed firstly with 10% sodium carbonate solution and then with water. The organic phase is dried and evaporated. The residue is chromatographed on silica gel while eluting with ether/hexane. There are obtained 5.6 g of 2-(cholest-5-en-3β-yloxy)-1-ethanol, m.p. 92°-95° C., the starting material in Example 2q.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05215972 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-5a9fc99a148440379570455c8712019d |
| Source note | uspto-grants-1993_06 |