Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907373Generated: November 2, 2026

Pyridine → 4-(4-Methoxyphenyl)-1-(toluene-4-sulfonyl)piperidine

https://huagongshe.com/reaction/1907373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-(4-Methoxyphenyl)piperidineHCID 10679270—
SolventWaterHCID 962—
Product4-(4-Methoxyphenyl)-1-(toluene-4-sulfonyl)piperidineHCID 5748255266.2%

Reaction Steps

p-Toluenesulfonyl chloride (4.39 g, 23 mmol) was added to a pyridine solution (30 ml) of 4-(4-methoxyphenyl)piperidine (4.0 g, 21 mmol) and the mixture was stirred at room temperature overnight. Water was added to the solution mixture, which was then extracted with ethyl acetate. The organic phase was washed with hydrochloric acid and water, dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1). The purified product was concentrated to dryness under reduced pressure to obtain 4-(4-methoxyphenyl)-1-(toluene-4-sulfonyl)piperidine (4.8 g) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598162B2
Source datasetuspto-grants-2013_12
ORD IDord-9463e5b98b5f4957bfd55e2fefdaaee0
Source noteuspto-grants-2013_12