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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891794Generated: October 31, 2026

Dimethylformamide → 2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehyde

https://huagongshe.com/reaction/1891794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-Fluoro-4-hydroxybenzaldehydeHCID 587246—
Reactant2-(Chloromethyl)-5-fluoropyridineHCID 21698059—
SolventWaterHCID 962—
Product2-Fluoro-4-(5-fluoro-pyridin-2-ylmethoxy)benzaldehydeHCID 5925535642.2%

Reaction Steps

To an N,N-dimethylformamide (20.0 mL) solution of 2-fluoro-4-hydroxy-benzaldehyde (1.48 g, 10.2 mmol) was added sodium hydride (411 mg, 10.3 mmol, 60% in oil) under nitrogen atmosphere at 0° C., which was stirred for 20 minutes at room temperature. 2-Chloromethyl-5-fluoro-pyridine (1.20 g, 8.56 mmol) described in Manufacturing Example 41-1-2 was then added at room temperature, and stirred for 30 minutes at 80° C. Water was added at room temperature to the reaction solution, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:5→1:2) to obtain the title compound (901 mg, 42.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-db566dc6d21a4be29d85930befba7aeb
Source noteuspto-grants-2013_08