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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566014Generated: October 29, 2026

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

https://huagongshe.com/reaction/566014

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 numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-508742d8bf7e45b8a757c618091e7d54
Source noteuspto-grants-2001_01