HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208869Generated: November 1, 2026
Nitric Acid → 5-Bromo-2-methyl-3-nitrobenzoic acid
https://huagongshe.com/reaction/2208869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-Bromo-2-methylbenzoic acid | HCID 346004 | — |
| Product | 5-Bromo-2-methyl-3-nitrobenzoic acid | HCID 13770008 | 92% |
Reaction Steps
A solution of 5-bromo-2-methylbenzoic acid (5.0 g, 23 mmol) in concentrated H2SO4 (27 ml, 512 mmol) was cooled to 5° C. in an acetone/ice bath. A mixture of concentrated nitric acid (1.9 ml, 30 mmol) and concentrated H2SO4 (2.8 ml, 52 mmol) was added dropwise to the reaction mixture at −5 t0° C. over 15 minutes. The yellow reaction mixture was stirred at −5° C. for 2 hours during which time a yellow precipitate formed. The reaction mixture was poured onto ice (150 g) and the precipitate was then collected by filtration. The precipitate was air dried to give the title compound (5.5 g, 52%) as a pale yellow solid.; 1HNMR (500 MHz, DMSO-d6) δ ppm 8.29 (s, 1H) 8.13 (d, J=1.58 Hz, 1H) 2.43 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376422B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-d4165fe27c5a43828b4a051f6686db21 |
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| Source note | uspto-grants-2016_06 |
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