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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15037Generated: October 27, 2026

p-Toluenesulfonic acid → 2-Bromo-5-(2-tetrahydropyranyloxy)pyridine

https://huagongshe.com/reaction/15037

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant2-Bromo-5-hydroxypyridineHCID 2762865—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2-Bromo-5-(2-tetrahydropyranyloxy)pyridineHCID 8661489155%

Reaction Steps

A mixture of 2-bromo-5-hydroxypyridine (1.0 g, 5.75 mmols), 3,4-dihydro-2H-pyran (0.80 mL, 8.77 mmols) and p-toluenesulfonic acid (110 mg, 0.578 mmol) was stirred overnight in dichloromethane (20 mL) at room temperature. The reaction liquid was diluted with chloroform, washed with saturated brine and dried over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the resulting residue was purified on silica gel column chromatography (C-300; ethyl acetate:hexane=1:20-1:10) to provide the title compound (0.81 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732456B2
Source datasetuspto-grants-2010_06
ORD IDord-22d50e01a3bc4b4d88cece5f10779ccd
Source noteuspto-grants-2010_06