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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817172Generated: October 25, 2026

Sulfuric Acid → 4-Chloro-3-cyanobenzoic acid

https://huagongshe.com/reaction/1817172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium CyanideHCID 9032—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Amino-4-chlorobenzoic acidHCID 76092—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178418260HCID 178418260—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product4-Chloro-3-cyanobenzoic acidHCID 2264461219.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of conc. sulfuric acid (60 mL) and water (95 mL) containing 3-amino-4-chlorobenzoic acid (10.0 g, 57.1 mmol) was added sodium nitrite (10.0 g, 145 mmol) at 0° C. The mixture was stirred at 0° C. for 2 hours, and added to a stirred mixture comprising a mixture of water (250 mL) and benzene (175 mL) containing copper cyanide (7.1 g, 79.3 mmol), potassium cyanide (21.7 g, 333 mmol), potassium carbonate (285 g, 2.06 mmol) at a temperature not higher than 15° C. The resulting mixture was heated under stirring at 80° C. for one hour, cooled to room temperature, stirred under ice-cooling, and filtered using Celite to collect insolubles. The insolubles were washed with benzene (100 mL) and ether (100 mL). The aqueous portion was taken out, and made to pH 2 by addition of conc. hydrochloric acid under stirring and ice-cooling. The aqueous portion was subjected to extraction with ether (200 mL×2), dried over anhydrous sodium sulfate, and placed under reduced pressure to distill the solvent off. The residue was repeatedly purified by silica gel column chromatography (ethyl acetate/hexane), to obtain 2.0 g (yield 19%) of the titled compound as a pale yellow crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598254B2
Source datasetuspto-grants-2009_10
ORD IDord-9cc7396b0f3049e6ac5049ad0be4f3c7
Source noteuspto-grants-2009_10