Didecyldimethylammonium Chloride → Didecyldimethylammonium chloride iodopropargyl butylcarbamate
Reaction equation
[Cl-:1].[CH2:2]([N+:12]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])([CH3:14])[CH3:13])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[CH2:25]([NH:29][C:30](=[O:36])[O:31][CH:32]([I:35])[C:33]#[CH:34])[CH2:26][CH2:27][CH3:28].C([O-])(=O)C.C([N+](CCCCCCCCCC)(C)C)CCCCCCCCC>>[Cl-:1].[CH2:15]([N+:12]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])([CH3:14])[CH3:13])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24].[CH2:25]([NH:29][C:30](=[O:36])[O:31][CH:32]([I:35])[C:33]#[CH:34])[CH2:26][CH2:27][CH3:28]Participants
4
Procedure
The procedure of Example 173 was followed, substituting a mixture of 4 parts of didecyldimethylammonium chloride and 1 part of iodopropargyl butylcarbamate for the didecyldimethylammonium acetate.
Sources & evidence
- ORD record
- ord-3388e4b8a1ed4e1ea2aba933db07e4fa
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05641726
Reaction notes
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