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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051526Generated: November 1, 2026

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

https://huagongshe.com/reaction/2051526

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 numberUS05019568
Source datasetuspto-grants-1991_05
ORD IDord-b83dfa89d9124d0c9e4a19f333fa0f7a
Source noteuspto-grants-1991_05