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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 6-(5-Cholesten-3beta-yloxy)hexyl iodide | HCID 12805525 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(5-Cholesten-3beta-yloxy)-hexane-1-thiol | HCID 86737278 | 86.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04229441 |
|---|
| Source dataset | uspto-grants-1980_10 |
|---|
| ORD ID | ord-2f08834b8f5742f181bb8cb76eba6172 |
|---|
| Source note | uspto-grants-1980_10 |
|---|