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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118645Generated: November 1, 2026

p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid

https://huagongshe.com/reaction/2118645

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-(Nitromethylidene)-1-[(pyridin-4-yl)methyl]hexahydropyrimidineHCID 70249474—
SolventAcetoneHCID 180—
SolventChloroformHCID 6212—
Productp-Toluenesulfonic acidHCID 6101210.4%

Reaction Steps

Compound No. 1 (0.73 g) obtained in Example 1 was dissolved in a mixed solvent of acetone (10 ml) and chloroform (50 ml), and p-toluenesulfonic acid hydrate (0.63 g) was added. The mixture was vigorously shaken for 2 hours, and then allowed to stand at room temperature for 3 hours. The precipitated crystals were collected by filtration, and fully washed with acetone to give the p-toluenesulfonate (1.2 g) of compound No. 1 of this invention. mp. 170°-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04680294
Source datasetuspto-grants-1987_07
ORD IDord-320b7e5e8b3245f3bef16df40e9ff193
Source noteuspto-grants-1987_07