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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8972Generated: October 25, 2026

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

https://huagongshe.com/reaction/8972

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 numberUS07091217B2
Source datasetuspto-grants-2006_08
ORD IDord-7a2f34a04f1b42dcbdbae8ab9077148c
Source noteuspto-grants-2006_08