HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(chloromethyl)-1-ethyl-5-methyl-1H-imidazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (1-ethyl-5-methyl-1H-imidazol-4-yl)methanol | HCID 54437975 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(chloromethyl)-1-ethyl-5-methyl-1H-imidazole hydrochloride | HCID 66820756 | 96% |
Reaction Steps
To a solution of (1-ethyl-5-methyl-1H-imidazol-4-yl)methanol (340 mg, 2.4 mmol) in anhydrous dichloromethane (20 mL) was added thionyl chloride (9004). The mixture was stirred at room temperature for 4 hours. Dichloromethane was evaporated, and the mixture was then co-evaporated with toluene (20 mL). The residue was dried in vacuo, affording 4-(chloromethyl)-1-ethyl-5-methyl-1H-imidazole hydrochloride (450 mg, 96% yield). The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315521B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-cc89ecf106494109b81b39669a90c7eb |
| Source note | uspto-grants-2016_04 |