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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157916Generated: November 2, 2026

Potassium Carbonate → 4-(1,3-Thiazol-2-yl)benzaldehyde

https://huagongshe.com/reaction/1157916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromothiazoleHCID 76430—
Reactant4-Formylphenylboronic AcidHCID 591073—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-(1,3-Thiazol-2-yl)benzaldehydeHCID 1053565515%

Reaction Steps

To a solution of 2-bromothiazole (0.26 g, 1.6 mmol) and 4-formylphenylboronic acid (0.48 g, 3.2 mmol) in toluene (16 mL) was added tetrakis(triphenylphosphine)palladium(0) (0.09 g, 0.08 mmol) and K2CO3 (0.33 g, 2.4 mmol) and the solution stirred at reflux for 16 h. The reaction was cooled to room temperature, diluted with water (50 mL) and ethyl acetate (50 mL). The organic layer was separated, washed with brine (30 mL), dried (MgSO4), filtered, concentrated and purified by column chromatography on silica gel (2% MeOH/CH2Cl2) to give 4-(2-thiazolyl)-benzaldehyde (45 mg, 15%). 1H NMR (CDCl3) δ 7.45 (d, 1H, J=3.0 Hz), 7.90 (d, 1H, J=3.0 Hz), 7.97 (d, 2H, J=7.8 Hz), 8.15 (d, 2H, J=7.2 Hz), 10.07 (s, 1H (CHO)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807694B2
Source datasetuspto-grants-2010_10
ORD IDord-88c4d146864b4202918bb6cb7fc6d7c2
Source noteuspto-grants-2010_10