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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479487Generated: October 30, 2026

Butyl iodide → 3-Bromo-6-butoxypicolinonitrile

https://huagongshe.com/reaction/1479487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-6-oxo-1,6-dihydropyridine-2-carbonitrileHCID 66875102—
SolventAcetoneHCID 180—
Product3-Bromo-6-butoxypicolinonitrileHCID 66875695—

Reaction Steps

A solution of 3-bromo-6-oxo-1,6-dihydropyridine-2-carbonitrile (from Example 15/Step 2) (1.0 eq.), potassium carbonate (1.3 eq.), and 1-iodobutane (1.2 eq.) in acetone (0.3 M) was stirred at 70° C. overnight. The solvent was concentrated en vacuo, and the resulting residue was taken up in water and ethyl acetate. The aqueous layer was extracted with ethyl acetate three times. The combined organic layers were washed with brine, dried over anhydrous MgSO4, and concentrated en vacuo. The crude product was purified by a COMBIFLASH® system (ISCO) using 0-30% ethyl acetate in hexane to give a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408907B2
Source datasetuspto-grants-2016_08
ORD IDord-12dbb2c9df1f48cbbf75a52fff9faa38
Source noteuspto-grants-2016_08