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14984-73-7

Basic Information
CAS No.: 14984-73-7
Name: Imidodisulfurylfluoride
Article Data: 17
Molecular Structure:
Molecular Structure of 14984-73-7 (Imidodisulfurylfluoride)
Formula: F2H N O4 S2
Molecular Weight: 181.141
Synonyms: Bis(fluorosulfonyl)amine;Bis(fluorosulfonyl)imide; Bis(fluorosulfuryl)imine; Imidobis(fluorosulfate);Imidobis(sulfuryl fluoride)
PSA: 97.07000
LogP: 1.55710
Synthetic route
999-97-3

1,1,1,3,3,3-hexamethyl-disilazane

A

420-56-4

trimethylsilyl fluoride

B

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
With fluorosulfonyl fluoride In acetonitrile at 20 - 90℃; for 3h; Autoclave;A n/a
B 98%
15873-42-4

bis(chlorosulfonyl)amine

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
With perfluorooctylsulfonyl fluoride; hydrogen fluoride at 65 - 70℃; for 15h; Time;95.3%
With hydrogen fluoride; dimethyl sulfate at 90℃; for 16h; Reagent/catalyst; Inert atmosphere;90%
With zinc(II) fluoride In acetic acid butyl ester at 25℃; for 6h; Product distribution / selectivity; Inert atmosphere;79%
999-97-3

1,1,1,3,3,3-hexamethyl-disilazane

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
With fluorosulfonyl fluoride In ethyl acetate at 100℃; for 3h; Solvent; Temperature; Autoclave;95%
15873-42-4

bis(chlorosulfonyl)amine

bismuth trifluoride

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
at 20℃; for 12h; Concentration; Inert atmosphere;90%
at 20 - 50℃;Ca. 93 g
15873-42-4

bis(chlorosulfonyl)amine

7664-39-3

hydrogen fluoride

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
With chlorosulfonic acid; isocyanate de chlorosulfonyle at 160℃; under 60006 Torr; for 0.25h; Reagent/catalyst; Temperature; Pressure; Time;89%
at 130℃; for 2h; Product distribution / selectivity; Autoclave;55%
7789-21-1

fluorosulphonic acid

A

14483-63-7

sodium fluorosulfonate

B

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
With sodium chloride In dichloromethane distn. of a react.-mixt. of urea and HSO3F under vac.; distillate dissolved in CH2Cl2; NaCl added; stirred for 6 h under reflux;; NaSO3F filtered off; filtrate cooled to -80°C; filtn., recrystn. (CFCl3, -80°C).;A n/a
B 87.8%
15873-42-4

bis(chlorosulfonyl)amine

zinc(II) fluoride

7664-41-7

ammonia

A

{Zn(NH3)4}(2+)*2Cl(1-)={Zn(NH3)4}Cl2

B

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
Stage #1: bis(chlorosulfonyl)amine; zinc(II) fluoride In acetic acid butyl ester at 25℃; for 6h; Inert atmosphere;
Stage #2: ammonia In acetic acid butyl ester; water Product distribution / selectivity;
A n/a
B 81%
7790-94-5

chlorosulfonic acid

5329-14-6

aminosulfonic acid

7783-42-8

thionyl fluoride

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
In 1,2-dichloro-ethane at 80℃; under 16501.7 Torr; for 17h; Solvent; Autoclave;77%
15873-42-4

bis(chlorosulfonyl)amine

7783-56-4

antimony(III) fluoride

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
In neat (no solvent) absence of air and moisture; slight excess amine, stirring for 4 h; fractional distn. (25°C, 0.01 Torr), decantation from residual SbCl3;70%

potassium bis(fluorosulfuryl)amide

7789-21-1

fluorosulphonic acid

14984-73-7

bis(fluorosulfonyl)amide

Conditions
ConditionsYield
In neat (no solvent) under dry N2; KN(SO2F)2 placed in dry Schlenk vessel and HSO3F added under stream of dry nitrogen; mixture stirred with a glass stick and allowed to stay for one hour; HN(SO2F)2 distilled off under vacuum; contains small amounts of HSO3F according to (19)F-NMR;62%
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