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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774737Generated: November 2, 2026

Sodium Hydroxide → 3-Bromo-5-(chloromethyl)pyridine

https://huagongshe.com/reaction/1774737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
Reactant(5-Bromo-3-pyridinyl)methanolHCID 2784733—
SolventDichloromethaneHCID 6344—
Product3-Bromo-5-(chloromethyl)pyridineHCID 1170125993.2%

Reaction Steps

To a solution of (5-bromopyridin-3-yl)methanol (3 g, 16.0 mmol) in DCM (15 mL) cooled to 0° C. was added thionylchloride (7.59 g, 63.8 mmol) dropwise and the reaction mixture was stirred at room temperature over night. The mixture was poured onto ice/water (20 mL), basified with NaOH conc. (8 mL) and extracted with EtOAc (2×50 mL). Combined organics were dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by silica gel flash chromatography eluting with a 0 to 40% EtOAc-Heptane gradient to give the title compound (3.08 g, 93%) as a white solid. MS: 206.0, 207.9 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260408B2
Source datasetuspto-grants-2016_02
ORD IDord-921d1432379b42479dd93a6de7f66998
Source noteuspto-grants-2016_02