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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381957Generated: October 31, 2026

Ethyl Acetate → 2-Benzoyl-pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/2381957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
ReactantDimethylacetamideHCID 31374—
Reactant(5-Bromo-pyrimidine-2-yl)-phenyl-methanoneHCID 67360359—
CatalystPotassium ferrocyanide trihydrateHCID 161067—
Catalystpalladium(II) acetateHCID 167845—
Product2-Benzoyl-pyrimidine-5-carbonitrileHCID 6855643342%

Reaction Conditions

Temperature150 °C

Reaction Steps

(5-Bromo-pyrimidine-2-yl)-phenyl-methanone (1.6 g, 6.08 mmol) is dissolved in dimethylacetamide (20 mL), and potassium hexacyanoferrate(II) trihydrate (0.57 g, 1.34 mmol) is added, followed by Na2CO3 (0.64 g, 6.08 mmol), and palladium (II) acetate (68 mg, 0.3 mmol). The mixture is heated to 150° C. under N2 for 3 h, and then cooled to rt. EtOAc (30 mL) is added and the mixture is filtered. The filtrate is washed with water (2×15 mL) and 5% aqueous NH4OH (15 mL), dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography eluting with 70% EtOAc in heptane to afford 2-benzoyl-pyrimidine-5-carbonitrile (0.53 g, 42%) as a solid. MS: 210 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-853f8fc10aab41e595ebdb867dacb79f
Source noteuspto-grants-2012_09