HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897661Generated: November 1, 2026
Potassium Nitrate → 1-Bromo-5-fluoro-2-methyl-4-nitrobenzene
https://huagongshe.com/reaction/1897661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 2-Bromo-4-fluorotoluene | HCID 74016 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1-Bromo-5-fluoro-2-methyl-4-nitrobenzene | HCID 53403286 | — |
Reaction Steps
To a solution of 2-bromo-4-fluoro-1-methylbenzene (5 g, 26.4 mmol) dissolved in conc. sulfuric acid (20 mL) was added potassium nitrate (2.67 g, 26.4 mmol) in sulfuric acid (5 mL) at 0° C. After stirring at 0° C. for 1 hr, the reaction was diluted with water, extracted with ethyl acetate (3×40 mL). The combined organic phases were washed with saturated sodium bicarbonate solution and brine sequentially, and then dried over Na2SO4. The crude product obtained after concentration was purified by silica gel column chromatography with mixed solvent hexanes/EtOAc (95/5) to afford 1-bromo-5-fluoro-2-methyl-4-nitrobenzene as an orange solid. 1H NMR (400 MHz, chloroform-d) δ 7.93 (d, 1H, J=7.6 Hz), 7.50 (d, 1H, J=10 Hz), 2.43 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519129B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-7dedfc3fba4f401d8f6a5f97b0b3dde6 |
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| Source note | uspto-grants-2013_08 |
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