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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521583Generated: October 31, 2026

Thionyl Chloride → 3-Bromo-5-(chloromethyl)pyridine

https://huagongshe.com/reaction/1521583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(5-Bromo-3-pyridinyl)methanolHCID 2784733—
SolventDichloromethaneHCID 6344—
Product3-Bromo-5-(chloromethyl)pyridineHCID 11701259—

Reaction Steps

To a cooled (0° C.) solution of (5-bromopyridin-3-yl)methanol (38.8 g, 0.206 mol) in dichloromethane (0.6 L) was added a solution of thionyl chloride (149 mL, 2.05 mol) in dichloromethane (200 mL). The resulting mixture was stirred at reflux overnight. The reaction was then concentrated under reduced pressure, and the resulting residue was recrystallized from diethyl ether to provide the title compound: LCMS m/z 206 [M+H]+; 1H NMR (300 MHz, d6-DMSO) δ 12.66 (s, 1H), 8.69-8.74 (m, 2H), 8.25 (s, 1H), 4.83 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073929B2
Source datasetuspto-grants-2015_07
ORD IDord-337dfeb0a5a04e36ae17d3b12539f65f
Source noteuspto-grants-2015_07