Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751799Generated: October 28, 2026

4-Toluenesulfonyl chloride → 1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine

https://huagongshe.com/reaction/1751799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventPyridineHCID 1049—
Product1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidineHCID 1573471385.6%

Reaction Steps

5 g tert-butyl 4-hydroxypiperidine-1-carboxylate are placed in 15 ml of pyridine, then 4.7 g p-toluenesulphonyl chloride are added batchwise. The reaction mixture is stirred at ambient temperature, after 12 hours it is poured onto ice water and the mixture obtained is stirred for a further hour at ambient temperature. The precipitated solid is suction filtered and dried. 7.5 g product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09161927B2
Source datasetuspto-grants-2015_10
ORD IDord-d2e0ce47cc3c4ee0bbd936f43df68a9e
Source noteuspto-grants-2015_10