HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576065Generated: October 31, 2026
Water → 2-(Difluoromethoxy)-4-fluoro-1-nitrobenzene
https://huagongshe.com/reaction/576065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 5-Fluoro-2-nitrophenol | HCID 9937 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl chlorodifluoroacetate | HCID 73935 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Difluoromethoxy)-4-fluoro-1-nitrobenzene | HCID 46311588 | 71.9% |
Reaction Steps
Potassium carbonate (2.42 g, 17.5 mmol) was added to a solution of 5-fluoro-2-nitrophenol (785 mg, 5.00 mmol) in N,N-dimethylformamide (10 mL), and the mixture was stirred at room temperature for 20 min. Chlorodifluoroacetic acid methyl ester (1.33 mL, 12.5 mmol) was added dropwise to the reaction mixture, and the mixture was stirred at room temperature for 30 min and then stirred at an external temperature of 90° C. for 3 hr. After cooling, water was added thereto and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine and dried over anhydrous magnesium sulfate and then the desiccant was filtered off, followed by concentration under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→4:1) to afford 2-(difluoromethoxy)-4-fluoro-1-nitrobenzene as a pale yellow oil (745 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035059B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-48b518a5ce6d439b97ab2c8b6ce45b97 |
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| Source note | uspto-grants-2015_05 |
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