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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | (5-Bromo-pyrimidine-2-yl)-phenyl-methanone | HCID 67360359 | — |
| Catalyst | Potassium ferrocyanide trihydrate | HCID 161067 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 2-Benzoyl-pyrimidine-5-carbonitrile | HCID 68556433 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258130B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-853f8fc10aab41e595ebdb867dacb79f |
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| Source note | uspto-grants-2012_09 |
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