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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050112Generated: October 26, 2026

Phosphorus oxychloride → 5-Bromo-2-chloro-3-ethoxypyridine

https://huagongshe.com/reaction/1050112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPyridine, 3-bromo-5-ethoxy-, 1-oxideHCID 53497593—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-chloro-3-ethoxypyridineHCID 7130367333.3%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 3-bromo-5-ethoxypyridine-1-oxide (40 g, 183 mmol) in DCM (200 mL) at 0° C. was slowly added POCl3 (159 mL, 1701 mmol) over 30 min. Then the resulting solution was warmed to 45° C. and stirred for 15 h. The mixture was concentrated and adjusted pH=9-10 with 10% NaOH solution, extracted with DCM (300 mL×2), dried over Na2SO4, filtered, and concentrated to give the crude product which was purified by silica column chromatography (10% EA: 90% PE, 800 g silica column). All fractions found to contain product by TLC (EA: PE=1:5, Rf=0.6) were combined and concentrated to yield an oil of 5-bromo-2-chloro-3-ethoxypyridine (30 g, 60.9 mmol, 33% yield): 1H NMR (400 MHz, CD3OD) δ 8.00-7.99 (d, J=2.0 Hz, 1H), 7.65-7.64 (d, J=2.0 Hz, 1H), 4.17-4.12 (m, 2H), 1.44 (t, J=7.0 Hz, 2H); ES-LCMS m/z 235 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382238B2
Source datasetuspto-grants-2016_07
ORD IDord-3c87d16ff2db42898743ad29f226be33
Source noteuspto-grants-2016_07