HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890811Generated: October 29, 2026
2-Bromopyrimidine → 4-(Pyrimidin-2-yl)benzaldehyde
https://huagongshe.com/reaction/890811
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopyrimidine | HCID 78345 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(Pyrimidin-2-yl)benzaldehyde | HCID 12703722 | 84.4% |
Reaction Steps
A solution of 2-bromopyrimidine (1.00 g, 6.3 mmol) and tetrakistriphenylphosphine(0) palladium (0.218 g, 0.189 mmol) in ethylene glycol dimethyl ether (30 mL) was stirred at room temperature for 10 minutes. A solution of 4-formylbenzene boronic acid (1.14 g, 7.61 mmol) and sodium bicarbonate (1.58 g, 18.9 mmol) in 15 mL water was added and the reaction was heated at reflux for 18 h. The mixture was diluted with water and CH2Cl2. The layers were separated, and the aqueous solution was washed with CH2Cl2. The combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified via flash chromatography (10% to 30% hexanes in EtOAc) to afford the title compound (0.979 g). 1H NMR (400 MHz, CDCl3) δ 10.11 (s, 1H), 8.83 (s, 2H), 8.82 (s, 1H), 7.98 (s, 2H), 7.23 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06998423B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-1da3be308a5344d68ce9da4342277c64 |
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| Source note | uspto-grants-2006_02 |
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