HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium bis((trifluoromethyl)sulfonyl)azanide → HCID 178483696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium bis((trifluoromethyl)sulfonyl)azanide | HCID 3816071 | — |
| Reactant | 1,1-Dichloro-N,N,N',N'-tetramethylmethanediamine | HCID 12544745 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178483696 | HCID 178483696 | 98.8% |
Reaction Steps
0.84 g (2.92 mmol) of lithium bis(trifluoromethanesulfonyl)imide in 4 ml of acetonitrile are added with stirring at room temperature to a solution of 0.5 g (2.92 mmol) of bis(dimethylamino)dichloromethane in 4 ml of acetonitrile. The mixture is stirred for 12 hours, and the solid LiCl is subsequently filtered off. Acetonitrile is distilled off. The crystals formed are dried at 50° C. under a reduced pressure of 10.0 Pa, giving 1.2 g of bis(dimethylamino)chlorocarbenium bis(trifluoromethanesulfonyl)imide, corresponding to a yield of 98.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07439395B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-6b823c7bcccd45fb84b20b90089e34af |
| Source note | uspto-grants-2008_10 |