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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903978Generated: October 26, 2026

Thiourea → 6-(5-Cholesten-3beta-yloxy)-hexane-1-thiol

https://huagongshe.com/reaction/903978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant6-(5-Cholesten-3beta-yloxy)hexyl iodideHCID 12805525—
SolventTetrahydrofuranHCID 8028—
Product6-(5-Cholesten-3beta-yloxy)-hexane-1-thiolHCID 8673727886.5%

Reaction Steps

Thiourea (7.5 g) is added to a solution of 6-(5-cholesten-3β-yloxy)hexyl iodide (15 g, 25.3 mmol) in tetrahydrofuran (200 ml) and the mixture is heated with stirring under reflux for 6 hours. The solution is concentrated to a residue which is triturated with anhydrous ether. The solid is filtered and dissolved in chloroform (100 ml). This solution is added to a solution of potassium metabisulfite (15 g) in water (100 ml). The mixture is heated under reflux in a nitrogen atmosphere for 20 minutes. The organic layer is washed with water, dried, and concentrated to dryness. The crude material is put on a silica gel column and eluted with 5% ethyl ether in peteroleum ether. The dried fractions are pooled and concentrated to give the title compound (11 g, 86% yield), m.p. 89°-90°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229441
Source datasetuspto-grants-1980_10
ORD IDord-2f08834b8f5742f181bb8cb76eba6172
Source noteuspto-grants-1980_10