HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942148Generated: October 25, 2026
Water → 3-fluoro-N-(4-methoxyphenyl)-2-nitroaniline
https://huagongshe.com/reaction/1942148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Difluoro-2-nitrobenzene | HCID 87922 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-fluoro-N-(4-methoxyphenyl)-2-nitroaniline | HCID 55100363 | 64.2% |
Reaction Steps
20.0 g (126 mmol) of 2,6-difluoronitrobenzene and 17.0 g (138 mmol) of p-anisidine were dissolved in N,N-dimethylformamide (60 ml), and 20.8 g (150 mmol) of potassium carbonate was added thereto. The mixture was heated with stirring for 12 hours at 75° C. The reaction mixture was poured into water, and extracted with ethyl acetate. The extracted organic layer was washed with water, 10% hydrochloric acid, water, and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue thus obtained was purified by silica gel chromatography (developing solvent: ethyl acetate:hexane=1:9), to obtain 21.2 g (yield: 64%) of 3-fluoro-N-(4-methoxyphenyl)-2-nitroaniline as a brown liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389523B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-32478bc9497745548bc000700d20adbd |
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| Source note | uspto-grants-2013_03 |
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