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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484552Generated: October 29, 2026

4-Toluenesulfonyl chloride → HCID 15049040, compound

https://huagongshe.com/reaction/484552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 67747384HCID 67747384—
SolventDiethyl EtherHCID 3283—
SolventSodium HydroxideHCID 14798—
ProductHCID 15049040HCID 1504904067%

Reaction Steps

To a solution of trans-2-carboxymethoxy-cyclohexyl ammonium chloride (1.048 g, 5 mmoles) in 1N NaOH (15 ml), there was aded a solution of p-toluenesulphonyl chloride (1.048 g, 5.5 mmoles) in diethyl ether (20 ml). The mixture was vigorously stirred for 20 hours at room temperature. The aqueous phase was separated, washed with diethyl ether (20 ml), acidified with HCl 18% to pH 2 and extracted with diethyl ether (5×20 ml). The organic extracts were dried with MgSO4, the drying agent was filtered off and filtrate was evaporated in vacuo. The residue was recrystallized from diisopropyl ether. Thus, there were obtained 1.09 g (67%) of the title compound in the form of white crystals, melting point 56°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231216
Source datasetuspto-grants-1993_07
ORD IDord-e31b0eab13a2408d804c572897a23672
Source noteuspto-grants-1993_07