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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404704Generated: October 27, 2026

Hydrogen Bromide → 3-(4-Bromo-2-fluoro-phenoxy)-2,6-dimethyl-pyridine

https://huagongshe.com/reaction/404704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium NitriteHCID 23668193—
Reactant4-(2,6-Dimethyl-pyridin-3-yloxy)-3-fluoro-phenylamineHCID 59287321—
Catalystcopper(I) bromideHCID 24593—
SolventWaterHCID 962—
Product3-(4-Bromo-2-fluoro-phenoxy)-2,6-dimethyl-pyridineHCID 5928731189%

Reaction Steps

A solution of sodium nitrite (4.57 g, 66.3 mmol) in water (75 ml) was added dropwise (over 45 minutes) to a cooled (at 0° C.) solution of intermediate D15 (7.7 g, 33.2 mmol) in 48% aqueous HBr (75 ml). The reaction mixture was warmed to room temperature and further stirred for 15 minutes, after which it was cooled again to 0° C. and copper(I) bromide (7.31 g, 49.8 mmol) was added portionwise. The mixture was allowed to reach room temperature, stirred for 15 minutes and finally it was heated at 140° C. for 1.5 hours. The reaction mixture was cooled to room temperature and neutralized with an aqueous saturated solution of potassium carbonate. EtOAc was added, the organic layer was separated and washed with brine, dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 0-10% EtOAc/heptane as eluent). The desired fractions were collected and evaporated in vacuo to yield D16 (8.75 g, 89%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748621B2
Source datasetuspto-grants-2014_06
ORD IDord-15c1c35e40ec4632a4d5c79df011fc81
Source noteuspto-grants-2014_06