HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 1-(4-Cyanobenzyl)-5-chloromethyl-2-methylimidazole hydrochloride salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(4-Cyanobenzyl)-5-hydroxymethyl-2-methylimidazole | HCID 21193415 | — |
| Product | 1-(4-Cyanobenzyl)-5-chloromethyl-2-methylimidazole hydrochloride salt | HCID 21193348 | — |
Reaction Steps
A mixture of 1-(4-cyanobenzyl)-5-hydroxymethyl-2-methylimidazole (3.45 g, 15.2 mmol) and thionyl chloride (30 mL, 411 mmol) was stirred at room temp. overnight under a calcium chloride drying tube. The resultant mixture was concentrated under vacuum, and residual thionyl chloride was removed by co-evaporation with toluene. The residue was triturated with anhydrous diethyl ether, filtered, washed with ether to provide the title compound as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248756B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-4ac8f2a410e64afbb3e389b1be355637 |
| Source note | uspto-grants-2001_06 |