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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266851Generated: October 26, 2026

Potassium Cyanide → 3-Cyano-5-nitrobenzoic acid

https://huagongshe.com/reaction/266851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantSodium CarbonateHCID 10340—
Reactant3-Amino-5-nitrobenzoic acidHCID 239342—
ReactantSodium NitriteHCID 23668193—
CatalystCopper SulfateHCID 24462—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product3-Cyano-5-nitrobenzoic acidHCID 2194256594%

Reaction Steps

3-Amino-5-nitrobenzoic acid (3.64 g, 20 mM) was dissolved in concentrated hydrochloric acid (20 ml), diluted with water (75 ml), cooled to 0°, and added over 30 minutes to a solution of NaNO2 (1.38 g, 20 mM) in water (10 ml). The pH was adjusted to 6.2 with saturated Na2CO3 solution. A mixture of CuSO4. 5H2O (10 g, 42 mM) in water (40 ml) and KCN (10 g, 154 mM) in water (20 ml) was heated to 65°, the solution of diazonium salt added over 15 minutes, and the mixture refluxed for 40 minutes. After cooling, and acidifying with 2M hydrochloric acid, the organics were extracted into ethyl acetate (2×200 ml). The combined extracts were washed with aqueous NaH2PO4, water, brine, and dried over Na2SO4. Evaporation gave 3-cyano-5-nitrobenzoic acid (3.6 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652233
Source datasetuspto-grants-1997_07
ORD IDord-dcd00c8064324d9b9546e5245b969aa8
Source noteuspto-grants-1997_07