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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21516Generated: October 25, 2026

Water → Methyl {o-{5-{[3-chloro-5-(trifluoromethyl)-2-pyridyl]oxy}-2-nitrophenoxy}phenoxy}acetate

https://huagongshe.com/reaction/21516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
ReactantMethyl [o-(5-hydroxy-2-nitrophenoxy)phenoxy]acetateHCID 54060386—
SolventDimethylformamideHCID 6228—
ProductMethyl {o-{5-{[3-chloro-5-(trifluoromethyl)-2-pyridyl]oxy}-2-nitrophenoxy}phenoxy}acetateHCID 5423822527.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl [o-(5-hydroxy-2-nitrophenoxy)phenoxy]acetate (1.9 g, 5.9 mmol), 2,3-di-chloro-5-(trifluoromethyl)pyridine (1.92 g, 8.9 mmol) and potassium carbonate (1.23 g, 8.9 mmol) in N,N-di-methylformamide is heated at 100° C. for 12 hours, cooled to room temperature, poured into water and extracted with ether. The organic extract is washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a yellow oil. Flash chromatography of the oil using silica gel and a (1:4) ethyl acetate/hexanes solution gives the title product as a yellow liquid (0.8 g) which is identified by 1HNMR and 13CNMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424280
Source datasetuspto-grants-1995_06
ORD IDord-0ea58b021f504387a450c1fee6fddaa9
Source noteuspto-grants-1995_06