HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800866Generated: November 2, 2026
Lithium bis((trifluoromethyl)sulfonyl)azanide → HCID 131730140, compound
https://huagongshe.com/reaction/1800866
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium bis((trifluoromethyl)sulfonyl)azanide | HCID 3816071 | — |
| Reactant | HCID 22406041 | HCID 22406041 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131730140 | HCID 131730140 | — |
Reaction Steps
Procedure 1c—A slight excess of lithium bis(trifluoromethylsulfonyl)imide dissolved in water was added to an aqueous solution of 1-butyl-1-methyl-azepanium iodide and stirred at room temperature for approximately 5 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 liquid, 1-butyl-1-methylazepanium bis(trifluoromethylsulfonyl)imide. δH (500.13 MHz, CDCl3) 3.42 (2H, m), 3.36 (2H, m), 3.22 (2H, m), 3.02 (3H, s), 1.88 (4H, m), 1.73 (6H, m), 1.40 (2H, sextet), 1.00 (3H, t). δC (125.76 MHz, CDCl3) 120 (q, CF3), 65.56, 64.84, 50.55, 27.46, 24.49, 21.80, 19.54, 13.37. ESI-MS: m/z=170 [M]+ (100). Calcd. for C11H24N: 170.1909; found: 170.1912, m/z=280 [M]− (100). Calcd. for C2F6NO4S2: 279.9173; found: 279.9163; Tg=−80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08345407B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-072f78709118402e93d8576f9e2cd688 |
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| Source note | uspto-grants-2013_01 |
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