Binary or ternary fluorine-containing sulfimide alkali metal salt and ionic liquid and applications thereof
A technology of fluorosulfonimide base and fluorosulfonimide, which is applied in the field of preparation of alkali metal salts and ionic liquids
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Embodiment 1
[0089] Embodiment 1: two (chlorosulfonyl) sulfonyl diimides (H 2 [(ClSO 2 N) 2 SO 2 ]) preparation
[0090] The synthesis reaction scheme is as follows:
[0091] NH 2 SO 2 NH 2 +SOCl 2 +ClSO 3 H→H 2 [(ClSO 2 N) 2 SO 2 ]+SO 2 +HCl
[0092] Add sulfuramide (NH 2 SO 2 NH 2 ) (48g, 0.5mol), SOCl 2 (167g, 1.4mol), ClSO 3 H (116 g, 1 mol). Stir magnetically, heat to 120°C and reflux for 24 hours, then distill under reduced pressure to collect fractions at 112-114°C / 1-2mm Hg. 135 g of colorless liquid was obtained, yield 92%.
Embodiment 2
[0093] Embodiment 2: (chlorosulfonyl) (perfluorobutylsulfonyl) sulfonyl diimide (H 2 [(ClSO 2 N)(C 4 f 9 SO 2 N) SO 2 ]) preparation
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[0095] Add the prepared C into the 250mL flask 4 f 9 SO 2 NHSO 2 NH 2 (37.8g, 0.1mol), SOCl 2 (16.7g, 0.14mol), ClSO 3 H (11.6 g, 0.1 mol). Heat to 120°C with stirring, reflux for 24 hours, and then distill under reduced pressure to collect fractions at 141-143°C / 1-2mm Hg. 40 g of product were obtained, yield 84%.
Embodiment 3
[0096] Example 3: Preparation of binary fluorine-containing sulfonimide and ternary fluorine-containing sulfonimide
[0097] The preparation conditions and experimental results of some binary fluorine-containing sulfonimides and ternary fluorine-containing sulfonimides are listed in Table 1.
[0098] Table 1 Experimental results for the preparation of binary and ternary fluorine-containing sulfonimides
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