HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37330Generated: October 29, 2026
p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid
https://huagongshe.com/reaction/37330
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | — |
Reaction Steps
The apparatus used in Example 1 was cleaned and charged with 95.1 g (0.50 mol) p-toluenesulfonic acid monohydrate and 750 mL toluene. The mixture was stirred to aid dissolution. MPP (88.13 g, 0.50 mol) was added slowly over 2 min. The reaction reached 38° C. The slurry was stirred for 1.5 hours, filtered, and the white solids allowed to air dry until partially dry (173.6 g). The solids were recrystallized from THF (approx. 1 L), filtered and dried. Dry weight=1782.1 g. Analysis by 1H NMR and FTIR verified the structure as that of the p-toluenesulfonic acid salt of MPP; mp=149°-150° C.; NaOH titration=108.83%; FW=348.48.g/mol; soluble in H2O, MeOH. DMSO and acetone. Calculated for C18H24N2O3S: C, 62.4%; H, 6.94%; N, 8.04%; S, 9.20%; O, 13.77%; Found: C, 62.075; H, 6.90%; N, 7.98%; S, 9.04%; O, 14.01%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420223 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-a060a70403824befaf8cb4dbe960adfa |
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| Source note | uspto-grants-1995_05 |
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