Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228204Generated: October 31, 2026

Potassium Carbonate → tert-butyl 6-(4-methylphenyl)-2H-1-benzopyran-3-carboxylate

https://huagongshe.com/reaction/2228204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl 6-bromo-2H-chromene-3-carboxylateHCID 10566979—
Reactant4-Methylphenyl borateHCID 86645333—
CatalystHCID 178418397HCID 178418397—
SolventToluene-ethanol waterHCID 66602552—
Producttert-butyl 6-(4-methylphenyl)-2H-1-benzopyran-3-carboxylateHCID 1061582174.1%

Reaction Steps

Under argon atmosphere, a solution of tert-butyl 6-bromo-2H-1-benzopyran-3-carboxylate (5.00 g), 4-methylphenyl borate (2.62 g) and potassium carbonate (4,44 g) in toluene-ethanol-water (160-16-16 ml) was stirred at room temperature for 1 hour. To the reaction mixture was added tetrakistriphenylphosphinepalladium (0.56 g), and the mixture was refluxed for 14 hours and cooled to room temperature. The organic layer was washed with saturated sodium chloride solution, dried with magnesium sulfate and concentrated. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1:19) to give pale yellow crystals, which were recrystallized from ethanol to give tert-butyl 6—(4-methylphenyl)-2H-1-benzopyran-3-carboxylate (3.84 g) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-5902d1adad96486ebc7e74f1b41eebc5
Source noteuspto-grants-2002_07