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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-Fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzene | HCID 66998789 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Fluoro-6-methoxyphenoxy)-4-methoxy-1-nitrobenzene | HCID 66999078 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897628B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-1923f80fd6924496bbe65db47d37b4ac |
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| Source note | uspto-grants-2011_03 |
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