p-Toluenesulfonic acid monohydrate → p-Toluenesulfonate
Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:12][C:13]1[N:18]([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:28])([F:27])[F:26])[CH:20]=2)[C:17](=[O:29])[C:16]([C:30]([NH:32][CH2:33][C:34]2[CH:39]=[CH:38][C:37]([S:40]([CH3:43])(=[O:42])=[O:41])=[CH:36][N:35]=2)=[O:31])=[CH:15][C:14]=1[C:44]1[N:48]([CH3:49])[N:47]=[CH:46][CH:45]=1.O.[C:51]1([CH3:61])[CH:56]=[CH:55][C:54]([S:57]([OH:60])(=[O:59])=[O:58])=[CH:53][CH:52]=1>CC(C)=O>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:6][CH:7]=1.[CH3:12][C:13]1[N:18]([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([C:25]([F:27])([F:26])[F:28])[CH:20]=2)[C:17](=[O:29])[C:16]([C:30]([NH:32][CH2:33][C:34]2[CH:39]=[CH:38][C:37]([S:40]([CH3:43])(=[O:42])=[O:41])=[CH:36][N:35]=2)=[O:31])=[CH:15][C:14]=1[C:44]1[N:48]([CH3:49])[N:47]=[CH:46][CH:45]=1.[S:57]([C:54]1[CH:55]=[CH:56][C:51]([CH3:61])=[CH:52][CH:53]=1)([O-:60])(=[O:59])=[O:58]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
To compound (I) (5 g, 1.0 mol eq, limiting reagent) was charged acetone (150 mL, 30 rel vol). The temperature was adjusted to 55° C. and a solution formed. p-Toluenesulfonic acid monohydrate (1.77 g, 1.0 mol eq) was dissolved in acetone (10 mL, 2 rel vol). This solution was charged to the reaction. Following stirring and cooling, the solid was isolated by filtration, washed with acetone (10 mL, 2 rel vol) and dried to constant weight yielding compound (I) tosylate (5.98 g, 8.33 mmol, 91%).
Workup
- customwas adjusted to 55° C.
- customa solution formed
- additionThis solution was charged to the reaction
- temperaturecooling
- customthe solid was isolated by filtration
- washwashed with acetone (10 mL, 2 rel vol)
- customdried to constant weight
Sources & evidence
- ORD record
- ord-0e93a327e5554f83b61c7b7d48289c6e
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08232296B2
Reaction notes
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