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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252211Generated: November 3, 2026

4-Toluenesulfonyl chloride → 1-(p-Nitrobenzyloxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine

https://huagongshe.com/reaction/1252211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant1-(p-Nitrobenzyloxycarbonyl)-4-hydroxypiperidineHCID 13292709—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product1-(p-Nitrobenzyloxycarbonyl)-4-(p-toluenesulfonyloxy)piperidineHCID 13292710—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1-(p-nitrobenzyloxycarbonyl)-4-hydroxypiperidine (10.54 g) in dry pyridine (105 ml) was added p-toluenesulfonyl chloride (14.35 g) at 0° C., followed by stirring at 25° C. for 23 hours. The reaction mixture was diluted with water and extracted with diethyl ether-dichloromethane (9:1). The extract was washed successively with saturated aqueous sodium chloride, 1N hydrochloric acid, saturated aqueous sodium chloride and saturated aqueous sodium bicarbonate, dried over anhydrous sodium suflate and evaporated to give 1-(p-nitrobenzyloxycarbonyl)-4-(p-toluenesulfonyloxy)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742052
Source datasetuspto-grants-1988_05
ORD IDord-82d664200f304f5ca8b05ea2231f7c20
Source noteuspto-grants-1988_05