HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium methyl sulfate → 1,3-Dimethyl-2-chloroimidazolidinium methylsulfate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium methyl sulfate | HCID 2735086 | — |
| Reactant | 2,2-Dichloro-1,3-dimethylimidazolidine | HCID 12755676 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,3-Dimethyl-2-chloroimidazolidinium methylsulfate | HCID 86613035 | 94.2% |
Reaction Steps
3.00 g (17.75 mmol) of 1,3-dimethyl-2,2-dichloroimidazolidine and 2.38 g (17.75 mmol) of sodium methylsulfate are mixed with 20 ml of dry acetonitrile. The reaction mixture is stirred for 5 hours at room temperature, and the precipitate NaCl is filtered off. The solvent is distilled off, and the residue is dried for 1 hour under a reduced pressure of 7 Pa and at 50° C., giving 4.09 g of 1,3-dimethyl-2-chloroimidazolidinium methylsulfate as a viscous material, corresponding to a yield of 94.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07439395B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-8a66758521a44f5ab15978a0d5deb961 |
| Source note | uspto-grants-2008_10 |