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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258557Generated: November 1, 2026

Pyridine → 6-Bromo-2-(bromomethyl)-3-fluoropyridine

https://huagongshe.com/reaction/1258557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl bromideHCID 68176—
Reactant(6-Bromo-3-fluoropyridin-2-yl)methanolHCID 53485567—
SolventDichloromethaneHCID 6344—
Product6-Bromo-2-(bromomethyl)-3-fluoropyridineHCID 8664228595.8%

Reaction Steps

To a stirred solution thionyl bromide (2.44 g, 11.78 mmol, 1.05 eq.) in 50 ml dry DCM, cooled to 5° C., was added dropwise a solution of (6-bromo-3-fluoropyridin-2-yl)methanol (2.54 g, 11.22 mmol, 1 eq.) and pyridine (0.931 g, 11.78 mmol, 1.05 eq.) in 15 ml dry DCM. On complete addition, the cooling bath was removed, the reaction warmed to room temperature and stirred 1.5 hr. 150 ml of water and 150 ml of DCM were added and stirring allowed for 2 mins. The organic layer was separated, dried of MgSO4 and concentrated. The residue was purified by chromatography on silica gel to give 6-bromo-2-(bromomethyl)-3-fluoropyridine (2.89 g, 87% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466176B2
Source datasetuspto-grants-2013_06
ORD IDord-b3399bd5cf3e406985a575a82f1604e6
Source noteuspto-grants-2013_06