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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873929Generated: October 27, 2026

Potassium Cyanide → Methyl 2-chloro-4-cyanobenzoate

https://huagongshe.com/reaction/1873929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantNitrous AcidHCID 24529—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 4-Amino-2-chlorobenzoateHCID 11839197—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178418546HCID 178418546—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductMethyl 2-chloro-4-cyanobenzoateHCID 53845357—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Amino-2-chloro-benzoic acid methyl ester (25 g, 72.7 mmol) was dissolved in 10% aqueous H2SO4 (150 mL) and the solution was cooled to 0° C. A solution of NaNO2 (11.15 g, 16.88 mmol) in water (50 mL) was added dropwise maintaining the temperature between 0-5° C. The mixture was stirred for 10 min., excess nitrous acid was neutralized using a saturated aqueous NaHCO3 solution. The resulting mixture was then added to a precooled (0-5° C.) suspension of CuCN (13.87 g, 155 mmol) and KCN (10.07 g, 155 mmol) in water (200 mL). It was stirred for 10 min., then allowed to attain room temperature. It was stirred for 0.5 h and finally heated on a steam bath for 0.5 h. Excess saturated FeCl3 solution was then added to the reaction mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304449B2
Source datasetuspto-grants-2012_11
ORD IDord-a6d4ef0d67154d99ae579a84b567b2dd
Source noteuspto-grants-2012_11