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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616468Generated: November 1, 2026

Nitric Acid → 5-Bromo-2-methyl-3-nitrobenzoic acid

https://huagongshe.com/reaction/1616468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant5-Bromo-2-methylbenzoic acidHCID 346004—
Product5-Bromo-2-methyl-3-nitrobenzoic acidHCID 1377000892%

Reaction Conditions

Temperature-2.5 °C

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 to 0° C. over 15 minutes. The yellow reaction mixture was stirred at −5 to 0° 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. LC-MS 57%, 1.82 min (3.5 minute LC-MS method), no ionization; 1H NMR (500 MHz, DMSO-d6) δ ppm 8.29 (s, 1H) 8.13 (d, J=1.58 Hz, 1H) 2.43 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765732B2
Source datasetuspto-grants-2014_07
ORD IDord-4f8331b6a3544962802910b40dd0645a
Source noteuspto-grants-2014_07