p-Toluenesulfonic acid monohydrate → p-Toluenesulfonate

HRID 1517483Notes

Reaction equation

HRID 1517483 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

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

  1. customwas adjusted to 55° C.
  2. customa solution formed
  3. additionThis solution was charged to the reaction
  4. temperaturecooling
  5. customthe solid was isolated by filtration
  6. washwashed with acetone (10 mL, 2 rel vol)
  7. 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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