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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691195Generated: October 25, 2026

Dimethylformamide → 6-(Pyridin-3-yloxy)-pyridine-3-carbaldehyde

https://huagongshe.com/reaction/1691195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant3-HydroxypyridineHCID 7971—
ReactantSodium hydrideHCID 24758—
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
SolventWaterHCID 962—
Product6-(Pyridin-3-yloxy)-pyridine-3-carbaldehydeHCID 5925519336%

Reaction Steps

To a suspension of sodium hydride (407 mg, 8.48 mmol, 50% in oil) and N,N-dimethylformamide (45 mL) was added an N,N-dimethylformamide (5 mL) solution of 3-hydroxypyridine (806 mg, 8.48 mmol) at 0° C., which was stirred for 30 minutes. An N,N-dimethylformamide (5 mL) solution of 2-chloro-5-formylpyridine (1.0 g, 7.06 mmol) was added to this reaction mixture at the same temperature, which was stirred for 5 hours at 100° C. The reaction mixture was cooled to room temperature, and water was added thereto, which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate) to obtain the title compound (505.1 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-bcb173cd74e84dd4942d21464fc12783
Source noteuspto-grants-2012_04