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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073538Generated: October 26, 2026

Sodium Iodide → 6-(5-Cholesten-3beta-yloxy)hexyl iodide

https://huagongshe.com/reaction/1073538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantCholest-5-en-3beta-yl 6-(p-toluenesulfonyloxy)hexyl etherHCID 13799772—
SolventAcetoneHCID 180—
Product6-(5-Cholesten-3beta-yloxy)hexyl iodideHCID 12805525—

Reaction Steps

A solution of cholest-5-en-3β-yl 6-(p-toluenesulfonyloxy)hexyl ether (33 g, 51 mmol) and sodium iodide (16 g, 0.106 mol) in acetone (250 ml) was refluxed for 4 hours. The solvent was removed under reduced pressure, filtered, and the collected salts washed well with ether. The filtrate was evaporated and residual yellow oil boiled in hexanes (400 ml). The solution was decanted, concentrated to 200 ml, and stored in the refrigerator for two days. The product was filtered and the mother liquors concentrated to give a total yield of 30 g (97%), m.p. 103.5°-104.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970199
Source datasetuspto-grants-1990_11
ORD IDord-8098aa7318c1488a9262e475468fb7c6
Source noteuspto-grants-1990_11