Sodium 3-nitrobenzenesulfonate → HCID 19779027, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([S:10]([O-:13])(=[O:12])=[O:11])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[Na+].[Cl-].[Cl-].[C:17]([O:25][CH2:26][CH2:27][N+:28]([CH3:52])([CH3:51])[CH2:29][C:30]1[CH:35]=[CH:34][C:33]([CH2:36][N+:37]([CH2:40][CH2:41][O:42][C:43](=[O:50])[C:44]2[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=2)([CH3:39])[CH3:38])=[CH:32][CH:31]=1)(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>O>[N+:1]([C:4]1[CH:5]=[C:6]([S:10]([O-:13])(=[O:11])=[O:12])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[N+:1]([C:4]1[CH:5]=[C:6]([S:10]([O-:13])(=[O:11])=[O:12])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[C:17]([O:25][CH2:26][CH2:27][N+:28]([CH3:52])([CH3:51])[CH2:29][C:30]1[CH:31]=[CH:32][C:33]([CH2:36][N+:37]([CH2:40][CH2:41][O:42][C:43](=[O:50])[C:44]2[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=2)([CH3:38])[CH3:39])=[CH:34][CH:35]=1)(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 17.11 grams (0.076 mol) of sodium m-nitrobenzenesulfonate in 75 milliters of water was added to a solution of 21.34 grams (0.038 mol) N,N'-bis(2-benzoyloxyethyl)-N,N,N',N'-tetramethyl-p-xylylenebisammonium dichloride, prepared as described in Example 2, in 100 milliters of water. An oily precipitate formed which crystallized with stirring. the solid was collected, washed with water and recrystallized from 2-butanone. The yield of product was 21.7 rams (63.81% of theory); mp=180°-182° C.
Workup
- customprepared
- customAn oily precipitate formed which
- customcrystallized
- customthe solid was collected
- washwashed with water
- customrecrystallized from 2-butanone
Sources & evidence
- ORD record
- ord-2566f7c0e86a4eefaafeb708d2a82355
- Source dataset
- uspto-grants-1993_02
- Patent number
- US05187037
Reaction notes
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