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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885684Generated: October 30, 2026

Nitric Acid → HCID 59560629, compound

https://huagongshe.com/reaction/885684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-bromo-4-fluorobenzoateHCID 7210837—
ReactantBenzoic acid, 2-bromo-4-fluoro-5-nitro-, methyl esterHCID 43449031—
SolventEthyl AcetateHCID 8857—
ProductHCID 59560629HCID 5956062943%

Reaction Steps

2-Bromo-4-fluoro-5-nitro-benzoic acid methyl ester. To conc. fuming H2SO4 (8 mL) at 0° C. was added conc. fuming HNO3 (8 mL) and the mixture allowed to stand for 5 min. To a solution of 2-bromo-4-fluoro-benzoic acid methyl ester (9.32 g, 40 mmol) at 0° C., the mixture of acids was added dropwise over 30 min. The mixture was allowed to warm to RT and was stirred for 18 h. The mixture was poured into ice water, diluted with EtOAc, and treated with 6 N NaOH. The aqueous layer was extracted with EtOAc (3×300 mL). The combined organic layers were washed with brine (200 mL), dried (MgSO4), and concentrated. The crude material was purified on SiO2 (0-25% EtOAc/hexanes) to provide 4.9 g (43%) of the title compound. 1H NMR (500 MHz, CDCl3): 8.61 (d, J=8.0, 1H), 7.66 (d, J=10.0, 1H), 3.91 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242275B2
Source datasetuspto-grants-2012_08
ORD IDord-56eebeac7a804b3997eea193f0d95179
Source noteuspto-grants-2012_08