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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262855Generated: November 2, 2026

Nitrogen → 4-Iodo-2-methoxynicotinaldehyde

https://huagongshe.com/reaction/2262855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl formateHCID 8025—
Reactant2-Fluoro-3-iodopyridineHCID 7009501—
ReactantSodium MethoxideHCID 10942334—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-Iodo-2-methoxynicotinaldehydeHCID 1003838164.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of diisopropylamine (345 mL, 249 g, 2.46 mol) in anhydrous THF (5 L) at −8 to −10° C. under a blanket of N2 was added n-BuLi (880 mL, 158 g, 2.46 mol) dropwise via cannula. The mixture was stirred at −10° C. for 30 min, cooled to −78° C. and treated with a solution of 2-fluoro-3-iodopyridine (500 g, 2.24 mol) in dry THF (2 L) dropwise. After the addition, the reaction mixture was warmed to −60° C. and this temperature was maintained for 2 h. The mixture was then cooled to −78° C., treated with ethyl formate (183 g, 2.47 mol) dropwise, followed by sodium methoxide (149 g, 2.75 mol) in MeOH (1.5 L) and warmed to ambient temperature. The reaction mixture was quenched with ice water and extracted with EtOAc. The layers were separated and the organic phase was washed with water and brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel to afford 4-iodo-2-methoxynicotinaldehyde (380 g, 64%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851489B2
Source datasetuspto-grants-2010_12
ORD IDord-0d4949f5b1b948d4a7cd7237314663f6
Source noteuspto-grants-2010_12