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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598965Generated: October 30, 2026

Water → 2-(2-Fluoro-6-methoxyphenoxy)-4-methoxy-1-nitrobenzene

https://huagongshe.com/reaction/598965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium MethoxideHCID 10942334—
Reactant4-Fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzeneHCID 66998789—
SolventDimethylformamideHCID 6228—
Product2-(2-Fluoro-6-methoxyphenoxy)-4-methoxy-1-nitrobenzeneHCID 6699907870%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzene (1.33 g, 5 mmol) and sodium methoxide (035 g, 6 mmol) in DMF (10 ml) was heated at 80° C. for 2 h. The mixture was poured into water and was extracted with ethyl acetate (3×20 ml). The combined organic layer was washed with water, brine and dried (Na2SO4). The solution was concentrated under reduced pressure to obtain 2-(2-fluoro-6-methoxyphenoxy)-4-methoxy-1-nitrobenzene (1.02 g, 70%). This compound was reduced to 2-(2-fluoro-6-methoxyphenoxy)-4-methoxyaniline (0.62 g, 73%) following the general procedure C. N-[2-(2-Fluoro-6-methoxyphenoxy)-4-methoxyphenyl]-N′-(thiazol-2-yl)urea (136 mg, 70%) was prepared from 2-(2-methoxy-6-fluorophenoxy)-4-methoxyaniline (132 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897628B2
Source datasetuspto-grants-2011_03
ORD IDord-1923f80fd6924496bbe65db47d37b4ac
Source noteuspto-grants-2011_03