Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174328Generated: October 31, 2026

Hydrochloric Acid → 5-Bromo-2-chloro-4-fluorobenzoic acid

https://huagongshe.com/reaction/2174328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium NitrateHCID 24268—
Reactant2-Amino-5-bromo-4-fluoro-benzoic acidHCID 28827257—
CatalystCupric ChlorideHCID 24014—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-Bromo-2-chloro-4-fluorobenzoic acidHCID 5333045592%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-amino-5-bromo-4-fluorobenzoic acid (14.5 g, 62.2 mmol) in concentrated hydrochloric acid (30 mL) at 0° C. was added dropwise a solution of sodium nitrate (4.72 g, 68.4 mmol) in water (15 mL). The mixture was stirred at 0° C. for 2 hours, then diluted with 1,4-dioxane (40 mL) and added dropwise to a solution of copper chloride (7.4 g, 74.4 mmol) in concentrated hydrochloric acid (25 mL) under mechanical stirring while the reaction temperature was kept below 7° C. (ice-salt bath). After the addition was complete, the mixture was stirred at 0° C. for another 1 hour. Water was added, and the precipitate was filtered. The filter cake was washed with water and dissolved in ethyl acetate. The filtrate was extracted with ethyl acetate once and washed with water and then with brine. The combined organic layers were dried over sodium sulfate and concentrated to give the crude product 28 (14.5 g, 92%), which was used for the next step without further purification. MS ESI (m/z): 251 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061060B2
Source datasetuspto-grants-2015_06
ORD IDord-3ac6d78292614ae1955d6158e89957a2
Source noteuspto-grants-2015_06