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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005954Generated: November 3, 2026

Pyridine → 2-(5-Tosyloxy-pentyloxy)pyridine

https://huagongshe.com/reaction/1005954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-(5-Hydroxypentyloxy)pyridineHCID 12137118—
SolventDichloromethaneHCID 6344—
Product2-(5-Tosyloxy-pentyloxy)pyridineHCID 1213711954.6%

Reaction Steps

5 ml of pyridine and 7 g of p-toluenesulfonyl chloride were added to a solution of 6.5 g of the compound obtained in Example 3a in 20 ml of dichloromethane and then the mixture was stirred for 4 hours. The organic layer was washed with 10% aqueous citric acid and then with water and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (ethyl acetate) to obtain 6.57 g of the title compound (yield: 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787561B1
Source datasetuspto-grants-2004_09
ORD IDord-3b2996a94c454792a4f6f0e091413eaa
Source noteuspto-grants-2004_09