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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384645Generated: October 25, 2026

Thionyl Chloride → 3-(2-Chloroethoxy)pyridine hydrochloride

https://huagongshe.com/reaction/1384645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-(Pyridin-3-yloxy)ethan-1-olHCID 21908997—
SolventChloroformHCID 6212—
Product3-(2-Chloroethoxy)pyridine hydrochlorideHCID 2262498525.8%

Reaction Conditions

Temperature5 °C

Reaction Steps

Thionyl chloride (0.89 ml, 12 mmol) was added slowly to a solution of 3-(2-hydroxyethoxy)pyridine (1.13 g, 8 mmol) in trichloromethane (20 ml) at 5° C. The mixture was stirred at 5° C. for 1 hour and then at ambient temperature for 2 hours. The volatiles were removed by evaporation, the residue azeotroped with toluene and dried under vacuum to give 3-(2-chloroethoxy)pyridine hydrochloride (300 mg, 19%) as a solid. 1H NMR Spectrum: (DMSOd6) 3.99(t, 2H); 4.42(t, 2H); 7.82(dd, 1H); 8.05(dd, 1H); 8.42(d, 1H); 8.62(s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-aab8ae36889b4383ae6c0a660de451db
Source noteuspto-grants-2001_07