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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299721Generated: October 28, 2026

Sodium hydride → 4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]-benzaldehyde

https://huagongshe.com/reaction/2299721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantEthanol, 2-(methyl-2-pyrimidinylamino)-HCID 10419381—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDimethylformamideHCID 6228—
Product4-[2-(N-Methyl-N-(2-pyrimidinyl)amino)ethoxy]-benzaldehydeHCID 1003808972%

Reaction Steps

Sodium hydride (60% in oil, 4.40 g) was added to a solution of 2-(methyl-2-pyrimidylamino)ethanol (15.3 g) in N,N-dimethylformamide (400 ml) at room temperature under nitrogen atmosphere and stirred for 1 hour. A solution of 4-fluorobenzaldehyde (13.6 g) in N,N-dimethylformamide (100 ml) was added dropwise and stirred at room temperature for 15 hours. The reaction mixture was poured onto ice (200 g) and concentrated. The residue was dissolved in ethyl acetate, washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain 4-[2-(methyl-2-pyrimidylamino)ethoxy]benzaldehyde (18.4 g, yield 72%) as crystals from an ethyl acetate-hexane (1:1, v/v)-eluted fraction. Recrystallization from ethyl acetate-hexane gave colorless crystals. m.p. 74-75° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495581B1
Source datasetuspto-grants-2002_12
ORD IDord-dad48511e05d48519c64df00a3481977
Source noteuspto-grants-2002_12