HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941783Generated: November 2, 2026
Nitric Acid → 1-(2,3-Difluoro-5-nitrophenyl)ethanone
https://huagongshe.com/reaction/1941783
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 178466552 | HCID 178466552 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1-(2,3-Difluoro-5-nitrophenyl)ethanone | HCID 57475865 | 28% |
Reaction Steps
Under an inert atmosphere of nitrogen 1-(2,3-difluoro-phenyl)-ethanone (5.0 g (32 mmol) was added dropwise to sulphuric acid (95-97%, 20 ml), cooled to 0° C., at such a rate that the temperature was maintained below 5° C. Thereafter, the reaction mixture was cooled to −15° C. and a solution of nitric acid (3.22 ml, 46.4 mmol) in sulphuric acid (95-97%, 4.6 ml) was added dropwise at −15° C. After stirring at −10° C. for 45 minutes, the mixture was poured on ice. Ethyl acetate was added, then the organic layer separated, washed with water, dried over sodium sulphate, and evaporated at reduced pressure. Purification of the crude light yellow oil (5.64 g) by chromatography on silica gel using a gradient of heptane/ethyl acetate=100:0 to 0:100 yielded the 1-(2,3-difluoro-5-nitro-phenyl)-ethanone (1.83 g, 28% of theory) as a light yellow oil together with a mixture of 1-(2,3-difluoro-5-nitro-phenyl)-ethanone and 1-(2,3-difluoro-6-nitro-phenyl)-ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389513B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-82a723b392734ef39415a928ac534b32 |
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| Source note | uspto-grants-2013_03 |
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