Tetradecylamine → N-propyl-N'-tetradecylsulfamide
Reaction equation
[CH2:1]([NH2:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[CH2:16]([NH:19][S:20](Cl)(=[O:22])=[O:21])[CH2:17][CH3:18]>>[CH2:16]([NH:19][S:20]([NH:15][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])(=[O:22])=[O:21])[CH2:17][CH3:18]Participants
3
Procedure
The title compound was prepared following the method described Example 6. The starting reactants are 0.10 g (0.5 mmol) of N-tetradecylamine and 0.076 g (0.5 mmol) of N-propylsulfamoyl chloride. 0.092 g of a white solid are obtained. Yield 55%; m.p. 105-107° C.
Sources & evidence
- ORD record
- ord-d7bfbb58b3cf4b0084d1844684b7b43c
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188312B2
Reaction notes
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