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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827278Generated: November 1, 2026

2-Bromothiazole → 2-(1,3-Thiazol-2-yl)benzaldehyde

https://huagongshe.com/reaction/1827278

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiazoleHCID 76430—
Reactant2-Formylphenylboronic acidHCID 292189—
ReactantSodium BicarbonateHCID 516892—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(1,3-Thiazol-2-yl)benzaldehydeHCID 15532482—

Reaction Steps

To a mixture of 2-bromothiazole (826 mg, 4.99 mmol) and tetrakis(triphenylphosphine) palladium (0) (175 mg, 0.151 mmol) in 1,2-dimethoxyethane (20 mL) was added 2-formylbenzeneboronic acid (0.9017 g, 6.01 mmol) and 1N aqueous NaHCO3 (8 mL). The resultant mixture was heated at reflux for 6 hrs. The reaction mixture was diluted with water and extracted with EtOAc (2×50 mL). The organic solution was dried over Na2SO4, filtered and concentrated. The crude product was purified by gradient flash chromatography (10% to 25% EtOAc in hexane) to yield 2-(2-thiazolyl)benzaldehyde as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053101B2
Source datasetuspto-grants-2006_05
ORD IDord-5d623c59fae242bcac1f00568476b5a4
Source noteuspto-grants-2006_05