HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033186Generated: October 25, 2026
Water → N-(2,5-Difluoro-4-nitrophenyl)acetamide
https://huagongshe.com/reaction/1033186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,5-Difluoro-4-nitroaniline | HCID 235930 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Catalyst | 2-Dimethylaminopyridine | HCID 21885 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2,5-Difluoro-4-nitrophenyl)acetamide | HCID 14624893 | 88.4% |
Reaction Steps
A mixture of 6.0 g (0.034 mole) of 2,5-difluoro-4-nitroaniline, 6.5 g (0.064 mole) of acetic anhydride, and approximately 0.1 g (0.0008 mole) of dimethylaminopyridine in 300 ml of methylene chloride was stirred and heated at reflux for two hours. The reaction mixture was allowed to cool and stir at room temperature for approximately 18 hours. The solvent was removed from the mixture by distillation under reduced pressure, leaving a residue. To this residue was added 32.5 g (0.318 mole) of acetic anhydride and several drops of concentrated sulfuric acid. This mixture was stirred at room temperature for approximately 18 hours. Approximately 300 ml of water was added to the mixture causing a vigorous exotherm and a solid to form. This solid was collected by filtration. The filter cake was washed with water and was dried under reduced pressure to yield 6.5 g of N-(2,5-difluoro-4-nitrophenyl)acetamide. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05310724 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-577bd73ef8644ddb9ec7a279ccfeae41 |
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| Source note | uspto-grants-1994_05 |
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