HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-Chloromethyl-2-(4-chlorophenyl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [2-(4-Chlorophenyl)thiazol-5-yl]methanol | HCID 59562416 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloromethyl-2-(4-chlorophenyl)thiazole | HCID 59562485 | 92.8% |
Reaction Steps
To a suspension of [2-(4-chlorophenyl)thiazol-5-yl]methanol (3.24 g, 14.3 mmol) in dichloromethane (40 ml) is added dropwise the thionyl chloride (1.3 ml, 18 mmol) at room temperature under nitrogen. The reaction mixture is stirred at room temperature for 4 hours. Silica gel is added to the crude reaction mixture, the solvent is evaporated under reduced pressure and the residue is purified by flash chromatography on silica gel to give 5-chloromethyl-2-(4-chlorophenyl)thiazole (3.24 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08956999B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-0b240d2eaf9645ea991853f99463f79f |
| Source note | uspto-grants-2015_02 |