Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48485Generated: October 26, 2026

Nitric Acid → 2-Chloro-4-fluoro-5-nitrobenzoic Acid

https://huagongshe.com/reaction/48485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant2-Chloro-4-fluorobenzoic acidHCID 75259—
SolventHydrochloric AcidHCID 313—
Product2-Chloro-4-fluoro-5-nitrobenzoic AcidHCID 721082886.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

First, 50 g (0.29 mol) of 2-chloro-4-fluorobenzoic acid was dissolved in 150 ml of hydrochloric acid at room temperature, to which a mixed acid of 28 ml (0.31 mol) of fuming nitric acid and 56 ml of concentrated sulfuric acid was added dropwise at 35° to 45° C. Then, the solution was stirred at 40° C. for 1 hour and poured into 250 ml of ice-water. The precipitated crystals were collected by filtration and recrystallized from a mixed solution of hexane and ethyl acetate, which afforded 55 g (0.25 mol) of 2-chloro-4-fluoro-5-nitrobenzoic acid. Then, 55 g (0.25 mol) of 2-chloro-4-fluoro-5-nitrobenzoic acid was dissolved in 50 ml of ethyl acetate, to which 33 g (0.28 mol) of thionyl chloride was added, and the mixture was heated under reflux for 3 hours and then allowed to stand for cooling to room temperature. Then, 20 ml of ethanol and 30 g of triethylamine were added under ice cooling, and the mixture was stirred at room temperature for 2 hours. The solvent was distilled out, and the residue was purified by silica gel chromatography, which afforded 57 g (0.23 mol) of ethyl 2-chloro-4-fluoro-5-nitrobenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703503B2
Source datasetuspto-grants-2004_03
ORD IDord-f5fb7feea6c44a198f4e921881582a71
Source noteuspto-grants-2004_03