Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349968Generated: October 30, 2026

Thionyl Chloride → 3-(Chloromethyl)-5-phenylpyridine

https://huagongshe.com/reaction/349968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(5-Phenylpyridin-3-yl)methanolHCID 22254272—
Product3-(Chloromethyl)-5-phenylpyridineHCID 1108492586%

Reaction Steps

A mixture of 5-phenyl-3-pyridylmethanol (4.50 g) and thionyl chloride (5 ml) was stirred at room temperature for 1 hour. After the reaction mixture was concentrated, saturated aqueous sodium bicarbonate solution was added to the mixture, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The residue was subjected to silica gel column chromatography to obtain 3-chloromethyl-5-phenylpyridine (4.28 g, yield 86%) as colorless crystals from the fraction eluted with tetrahydrofuran. This was recrystallized from ethyl acetate-hexane. Melting point: 75–76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-583ccf24496241aa95ca1e2fff858437
Source noteuspto-grants-2007_02