HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium N-methylmethanaminide → 1,3-Dimethyl-2-dimethylaminoimidazolidinium nitrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium N-methylmethanaminide | HCID 5152226 | — |
| Reactant | 1,3-Dimethyl-2-chloroimidazolidinium nitrate | HCID 69311037 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,3-Dimethyl-2-dimethylaminoimidazolidinium nitrate | HCID 69312383 | 92.3% |
Reaction Steps
3.00 g (15.34 mmol) of 1,3-dimethyl-2-chloroimidazolidinium nitrate and 0.78 g (15.29 mmol) of lithium dimethylamide are dissolved in 20 ml of acetonitrile under a protective-gas atmosphere (argon). The reaction mixture is stirred for 5 hours at room temperature, and LiCl is subsequently filtered off. The salt LiCl is washed with 5 ml of acetonitrile, and the organic phases are combined. The solvent is distilled off, and the residue is dried under reduced pressure at 7 Pa and 50° C., giving 2.91 g of 1,3-dimethyl-2-dimethylaminoimidazolidinium nitrate as a liquid, corresponding to a yield of 92.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07439395B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-5ffac93d34464dd4ac156e277a65eff1 |
| Source note | uspto-grants-2008_10 |