Sulfuryl chloride → N,N-diethylsulfamoyl chloride
Reaction equation
Cl.[CH2:2]([NH:4][CH2:5][CH3:6])[CH3:3].[S:7](Cl)([Cl:10])(=[O:9])=[O:8]>>[CH2:2]([N:4]([CH2:5][CH3:6])[S:7]([Cl:10])(=[O:9])=[O:8])[CH3:3]Participants
3
Procedure
A solution of diethylamine hydrochloride (1 g) in sulfuryl chloride (10 ml) was heated at 50° C. for 4 hours. The solution was allowed to cool to ambient temperature and sulfuryl cloride was evaporated in vacuo. To the residue were added ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to give diethylsulfamoyl chloride (720 mg) as a colorless oil.
Workup
- customsulfuryl cloride was evaporated in vacuo
- additionTo the residue were added ethyl acetate and water
- washThe organic layer was washed with brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-c9689078cce94203bc3f9664f4463d98
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06967197B2
Reaction notes
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