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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667746Generated: October 26, 2026

4-Toluenesulfonyl chloride → 3-(Piperidin-1-yl)propyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/1667746

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPiperidine-1-propanolHCID 66032—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product3-(Piperidin-1-yl)propyl 4-methylbenzene-1-sulfonateHCID 1794465964.6%

Reaction Steps

To a mixture of 0.286 g (2 mmole) of 3-piperidin-1-yl-propan-1-ol, and 2 mL of pyridine was added 0.001 g of 4-dimethylaminopyridine and 0.381 g (2 mmole) of p-toluenesulphonyl chloride. The mixture was stirred at ambient temperature overnight and then concentrated under reduced pressure. The residue was taken up in 20 mL of dichloromethane and washed once with 10 mL of saturated sodium bicarbonate, twice with 10 mL of water, and then brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 0.384 g of toluene-4-sulfonic acid 3-piperidin-1-yl-propyl ester as a pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044213B2
Source datasetuspto-grants-2011_10
ORD IDord-77f378ada5574d72a43764ca204d5005
Source noteuspto-grants-2011_10