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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604648Generated: October 31, 2026

Dimethylformamide → Methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate

https://huagongshe.com/reaction/1604648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant2-(4-Tert-butylthiazol-2-yl)benzofuran-5-yl trifluoromethanesulfonateHCID 19603684—
Reactant1,3-Bis(diphenylphosphono)propaneHCID 53851155—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
ProductMethyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylateHCID 19603836—

Reaction Conditions

Temperature70 °C

Reaction Steps

Carbon monoxide was introduced by bubbling to a mixture of 2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl trifluoromethanesulfonate (6.0 g), palladium acetate (99.7 mg), 1,3-bis(diphenylphosphono)propane (183 mg, 0.44 mmol) and triethylamine (4.13 ml) in a mixed solvent of methanol (15 ml) and N,N-dimethylformamide (30 ml) at room temperature for 1 hour. The mixture was warmed to 70° C. and stirred under carbon monoxide balloon for 3 hours. The resulting mixture was filtered through celite and the residue was washed with ethyl acetate. The filtrate and washing solution was combined and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using ethyl acetate-n-hexane as eluent to give methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate (3.92 g) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-438352edabd341d88dfbc1795d420f22
Source noteuspto-grants-1999_11