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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587143Generated: November 5, 2026

Ethylene Glycol → 2-(Cholest-5-en-3beta-yloxy)-1-ethanol

https://huagongshe.com/reaction/1587143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantWaterHCID 962—
ReactantCholesteryl tosylateHCID 10907651—
Solvent1,4-DioxaneHCID 31275—
Product2-(Cholest-5-en-3beta-yloxy)-1-ethanolHCID 1418733570.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215972
Source datasetuspto-grants-1993_06
ORD IDord-5a9fc99a148440379570455c8712019d
Source noteuspto-grants-1993_06