HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl mercaptan → 2-Benzylthio-3-iodopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-3-iodopyridine | HCID 7009501 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Benzylthio-3-iodopyridine | HCID 15036865 | — |
Reaction Steps
A solution of 34.0 g (0.15 mol) of 2-fluoro-3-iodopyridine and 18.6 g (0.15 mol) of benzylmercaptan in 250 ml of acetonitrile is heated under reflux with 22.8 g (0.165 mol) of potassium carbonate for 8 h. The mixture is cooled, the solvent is removed on a rotary evaporator, the residue is taken up in dichloromethane and the organic phase is washed with water. After drying with sodium sulfate, evaporating and distilling the oily residue in vacuo, 37.3 g (76% of theory) of 2-benzylthio-3-iodopyridine of boiling point 150°-153° C. at 0.1 mbar are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05494886 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-d3af7c60a6734aadac32a76a7f56030c |
| Source note | uspto-grants-1996_02 |