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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250499Generated: November 1, 2026

Benzene → N-(ethoxymethyl)-4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide

https://huagongshe.com/reaction/1250499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantChloromethyl ethyl etherHCID 18523—
ReactantSodium hydrideHCID 24758—
Reactant4-Methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamideHCID 18326229—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(ethoxymethyl)-4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamideHCID 18326199—

Reaction Steps

1.0 g (0.0032 mol) of 4-methoxy-6-{3-(trifluoromethyl)phenoxy}-2-pyridine carboxamide was dissolved in a mixed solvent containing about 20 ml of benzene and about 10 ml of DMF, and the obtained solution was mixed with 0.14 g (ca. 60% in mineral oil; 0.0032×1.1 mol) of NaH, followed by treating the solution under reflux for several minutes. Thereafter, the resultant reaction solution was mixed with 0.61 g (0.0032×2.0 mol) of chloromethyl ethyl ether, followed by treating the solution under reflux for about 3 hours. The reaction solution was distributed in ethyl acetate-saturated sodium bicarbonate water and then washed with saturated brine. The organic phase of the solution was dried with anhydrous sodium sulfate, concentrated and purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane), thereby obtaining an aimed product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339045B1
Source datasetuspto-grants-2002_01
ORD IDord-62b2204abffd4f3dad30fcadf711d46e
Source noteuspto-grants-2002_01