HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351856Generated: October 31, 2026
Acetic Acid → 2-Fluoro-4-nitrobenzoic acid
https://huagongshe.com/reaction/351856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Fluoro-4-nitrotoluene | HCID 74025 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Fluoro-4-nitrobenzoic acid | HCID 302679 | — |
Reaction Steps
Concentrated sulfuric acid (32 ml) was added carefully with stirring to a solution of 2-fluoro-4-nitrotoluene (16.5 g, 0.106 mol) in acetic acid (200 ml). The mixture was warmed up to 95° C., and solution of chromium trioxide (37.1 g, 0.371 mol) in water (32 ml) was added dropwise with stirring over 2 h. The mixture was heated with stirring for another 30 minutes, allowed to cool down to r.t., and poured into water (1000 ml). The product was extracted with diethyl ether (3×200 ml). Combined ether layers were washed with water and evaporated to dryness. The residue was dissolved in 10% aqueous potassium carbonate and washed with ether. The aqueous layer was acidified with con. HCl, and the resulting white precipitate filtered and dried (16.3 g, 83%), m.p. 174-177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743811B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-b3df808cf1f1436995c1566a6ebe5db3 |
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| Source note | uspto-grants-2004_06 |
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