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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500260Generated: November 3, 2026

(4-Methoxyphenyl)boronic acid → Ethyl 2-(4-methoxyphenyl)thiazole-4-carboxylate

https://huagongshe.com/reaction/1500260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantEthyl 2-bromo-1,3-thiazole-4-carboxylateHCID 353965—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantPotassium phosphate, tribasic, monohydrateHCID 22031701—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductEthyl 2-(4-methoxyphenyl)thiazole-4-carboxylateHCID 10400532—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Bromo-thiazole-4-carboxylic acid ethyl ester (1.00 mmol, 236 mg), 4-methoxyphenylboronic acid (1.50 mmol, 228 mg), Pd2(DBA)3 (0.020 mmol, 18 mg), S-Phos (0.060 mmol, 25 mg) and potassium phosphate tribasic monohydrate (1.5 mmol, 0.35 g) were loaded into a Schlenk tube containing a stir bar. The Schlenk tube was capped with a rubber septum, evacuated and refilled with nitrogen. Toluene (2 mL) was added through the septum via a syringe and the Schlenk tube was sealed with a Teflon screw cap under a flow of nitrogen, and put into an oil bath at 100° C. The reaction was allowed to stir at 100° C. for 15 hours, then the reaction mixture was cooled to room temperature and filtered through celite. The filtrate was concentrated in vacuo and the resultant crude residue was purified using column chromatography on silica gel (eluent: Hexane/EtOAc (4:1)) to provide 2-(4-Methoxy-phenyl)-thiazole-4-carboxylic acid ethyl ester as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206142B2
Source datasetuspto-grants-2015_12
ORD IDord-4d36a83c1e664bcbb7c3d57263cbbcc8
Source noteuspto-grants-2015_12