Ammonia → O-Benzenedisulfonimide

HRID 2108168Notes

Reaction equation

HRID 2108168 reaction equation
[NH3:1].[C:2]1([S:12](Cl)(=[O:14])=[O:13])[C:3]([S:8](Cl)(=[O:10])=[O:9])=[CH:4][CH:5]=[CH:6][CH:7]=1>C(O)C.C1(C)C=CC=CC=1>[S:12]1(=[O:14])(=[O:13])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[S:8](=[O:10])(=[O:9])[NH:1]1

Participants

5

Reactant 2

HCID 222AmmoniaHCID 246432Benzene-1,2-disulfonyl dichloride

Product 1

HCID 10500043O-BenzenedisulfonimideYield 91%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 1140TolueneSolvent

Procedure

A solution of 0.65 mol of ammonia in 1,050 ml of absolute ethanol is added dropwise, with stirring, to 0.13 mol of 1,2-benzenedisulphonyl chloride in 720 ml of absolute toluene at 25° C. The mixture is stirred a further hour, slight cloudiness is removed by filtration through a layer of kieselguhr, and the filtrate is evaporated to dryness. The ammonium salt of 1,3,2-benzodithiazole 1,1,3,3-tetroxide is obtained.

Workup

  1. customslight cloudiness is removed by filtration through a layer of kieselguhr
  2. customthe filtrate is evaporated to dryness

Sources & evidence

ORD record
ord-2e175655c351477e99c41385d3179600
Source dataset
uspto-grants-1990_06
Patent number
US04937343

Reaction notes

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