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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447027Generated: October 30, 2026

Potassium thiocyanate → HCID 57813637, compound

https://huagongshe.com/reaction/447027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium thiocyanateHCID 516872—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
ReactantMethyl 2-amino-3-nitro-5-(3-pyridinyl)benzoateHCID 59337640—
CatalystCuprous thiocyanateHCID 178514150—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductHCID 57813637HCID 57813637—

Reaction Steps

A suspension of 2-Amino-3-nitro-5-pyridin-3-yl-benzoic acid methyl ester (0.92 g, 3.37 mmol) in aqueous sulfuric acid (50% v/v, 9 ml) was stirred at ambient temperature for 1 h before being cooled in an ice bath and treated over 5 min with an aqueous sodium nitrite solution (20% w/v, 1.4 ml). The mixture was stirred in the cold for 1.5 h before being treated with a solution of potassium thiocyanate (0.42 g) in water (1.0 ml) in one portion. The resultant mixture was stirred in the cold for 15 min and then added to a suspension of copper (I) thiocyanate (0.71 g) in water (2.8 ml) whilst cooling in an ice-bath. The mixture was stirred in the cold for 2 h and then heated to 70° C. for 20 min. After cooling to ambient temperature, the mixture was poured into a saturated aqueous solution of sodium hydrogen carbonate (200 ml) and extracted with ethyl acetate (3×100 ml) which was washed with brine (200 ml) and dried (MgSO4). The solvent was removed in vacuo to give a residue which was purified by flash chromatography (silica) eluting with 80% to 100% ethyl acetate in 40-60 petroleum ether. The 3-Nitro-5-pyridin-3-yl-2-thiocyanato-benzoic acid methyl ester was obtained as a pale yellow solid (0.78 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481544B2
Source datasetuspto-grants-2013_07
ORD IDord-dbec663b5d324f419305491e943e2fa9
Source noteuspto-grants-2013_07