HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium bis((trifluoromethyl)sulfonyl)azanide → 6-Azonia-spiro[5,6]dodecane bis[(trifluoromethyl)sulfonyl]imide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium bis((trifluoromethyl)sulfonyl)azanide | HCID 3816071 | — |
| Reactant | 6-Azaspiro[5.6]dodecan-6-ium bromide | HCID 17365656 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Azonia-spiro[5,6]dodecane bis[(trifluoromethyl)sulfonyl]imide | HCID 60145280 | — |
Reaction Steps
A slight excess of lithium bis[(trifluoromethyl)sulfonyl]imide dissolved in water was added to an aqueous solution of 6-azonia-spiro[5,6]dodecane bromide and stirred at room temperature for several hours. The reaction mixture was transferred to a separating funnel and the heavy layer washed several times with water. The addition of a small amount of dichloromethane aided the separation of the aqueous and organic layer. The heavy organic layer was then evaporated to dryness leaving a pale yellow solid, 6-azonia-spiro[5,6]dodecane bis[(trifluoromethyl)sulfonyl]imide with a melting point of 96° C. ES/MS 168 (Cation C11H22N), −280 (Anion C2F6NS2O4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088917B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-b3ce2ab816f644c9bb7da91ace2f4949 |
| Source note | uspto-grants-2012_01 |