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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699076Generated: October 31, 2026

2-Bromopyrimidine → 4-(Pyrimidin-2-yl)benzaldehyde

https://huagongshe.com/reaction/1699076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyrimidineHCID 78345—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Formylphenylboronic AcidHCID 591073—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(Pyrimidin-2-yl)benzaldehydeHCID 1270372284.4%

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) δ10.11 (s,1H), 8.83 (s, 2H), 8.82 (s, 1H), 7.98 (s, 2H), 7.23 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344485B1
Source datasetuspto-grants-2002_02
ORD IDord-61edf676383345ba885a600b1940c0d7
Source noteuspto-grants-2002_02