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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium bis((trifluoromethyl)sulfonyl)azanideHCID 3816071—
ReactantHCID 22406041HCID 22406041—
SolventWaterHCID 962—
ProductHCID 131730140HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08345407B2
Source datasetuspto-grants-2013_01
ORD IDord-072f78709118402e93d8576f9e2cd688
Source noteuspto-grants-2013_01