HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium bis((trifluoromethyl)sulfonyl)azanide → 3-Ethyl-2-methylbenzothiazolium bis(trifluoromethanesulfonyl)imide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium bis((trifluoromethyl)sulfonyl)azanide | HCID 3816071 | — |
| Reactant | 3-Ethyl-2-methyl-1,3-benzothiazol-3-ium bromide | HCID 12859978 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Ethyl-2-methylbenzothiazolium bis(trifluoromethanesulfonyl)imide | HCID 131728831 | 88.7% |
Reaction Steps
2.22 g (7.73 mmol) of lithium bis(trifluoromethanesulfonyl)imide, Li[(CF3SO2)2N], in 5 ml of water are added dropwise with stirring to a solution of 2.00 g (7.75 mmol) of 3-ethyl-2-methylbenzothiazolium bromide in 50 ml of water. The lower liquid phase is extracted a number of times with 50 ml of dichloromethane, and the combined organic phases are dried using Mg2SO4. The solvent is subsequently removed by distillation, and the residue is dried under a reduced pressure of 1.3 Pa at 60° C., giving 3.14 g of 3-ethyl-2-methylbenzothiazolium bis(trifluoromethanesulfonyl)imide, corresponding to a yield of 88.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07939644B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-0574fb0a135e4658a9f6d5bd4eafa912 |
| Source note | uspto-grants-2011_05 |