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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421488Generated: November 4, 2026

p-Toluenesulfonate → p-Toluenesulfonic acid monohydrate

https://huagongshe.com/reaction/2421488

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ToluenesulfonateHCID 85570—
SolventMethanolHCID 887—
Productp-Toluenesulfonic acid monohydrateHCID 521998—

Reaction Conditions

Temperature25 °C

Reaction Steps

An aliquot (1.5 g, 2.2 mmol) of the tosylate anhydrous form 1 salt form of the compound of Formula I prepared above was dissolved in 4.5 mL of methanol. The solution was concentrated to dryness after 3 days by vacuum distillation. The solids were slurried in 4.5 mL of 2-propanol which was shaken at 25° C. and 350 RPM for six days yielding precipitate. The solids were collected by vacuum filtration and dried under vacuum at room temperature over a 12 hour period. The resulting crystalline tosylate hydrate form 2 salt form of the compound of Formula I was analyzed by X-ray crystallography (FIG. 21), DSC (FIG. 22), and TGA (FIG. 23) in accordance with the procedures described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956189B2
Source datasetuspto-grants-2011_06
ORD IDord-55ae6d00d33d4d0fb7789440b769612f
Source noteuspto-grants-2011_06