HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 5-(chloromethyl)-1-ethyl-4-methyl-1H-imidazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (1-ethyl-4-methyl-1H-imidazol-5-yl)methanol | HCID 59589441 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(chloromethyl)-1-ethyl-4-methyl-1H-imidazole hydrochloride | HCID 66820626 | 95% |
Reaction Steps
To (1-ethyl-4-methyl-1H-imidazol-5-yl)methanol (754 mg, 5.4 mmol) in anhydrous dichloromethane (35 mL) was added thionyl chloride (2 mL). The mixture was stirred at room temperature overnight. Dichloromethane was evaporated and then co-evaporated with toluene (2×15 mL). The residue was dried in vacuo, affording 5-(chloromethyl)-1-ethyl-4-methyl-1H-imidazole hydrochloride (1.0 g, 95% 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-caefa0a20113467e942638622639e02f |
| Source note | uspto-grants-2016_04 |