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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300571Generated: October 31, 2026

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

https://huagongshe.com/reaction/2300571

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(O) 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 hated at reflux for 16 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 on silica gel (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-c12df99d53b44a63882ec38da434564c
Source noteuspto-grants-2002_12