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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980613Generated: October 28, 2026

Pyridine → 5-(1-Benzyloxycarbonyl-4-piperidyl)pentylp-toluenesulfonate

https://huagongshe.com/reaction/980613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant5-(1-Benzyloxycarbonyl-4-piperidyl)pentanolHCID 14046930—
SolventEthyl AcetateHCID 8857—
Product5-(1-Benzyloxycarbonyl-4-piperidyl)pentylp-toluenesulfonateHCID 2014365366.5%

Reaction Steps

A mixture of 18 g of 5-(1-benzyloxycarbonyl-4-piperidy)pentanol and 150 ml of pyridine is stirred under ice-cooling, and 14.6 g of tosyl chloride is added portionwise to the mixture over the period of 30 minutes. After stirring for another 1 hour under ice-cooling, 2 ml of ice-cold water is added dropwise. Ethyl acetate (500 ml) is added to the reaction solution, which is then washed with 500 ml of 2 N-hydrochloric acid and 500 ml of 1 N hydrochloric acid successively, further with dilute aqueous sodium hydrogen-carbonate solution and water successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting oily material is purified by silica-gel column chromatography to give 18 g of 5-(1-benzyloxycarbonyl-4-piperidyl)pentyl p-toluenesulfonate as an oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04638000
Source datasetuspto-grants-1987_01
ORD IDord-1cb77232808249c9b566afb7e495d902
Source noteuspto-grants-1987_01