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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-butyl 6-bromo-2H-chromene-3-carboxylate | HCID 10566979 | — |
| Reactant | 4-Methylphenyl borate | HCID 86645333 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene-ethanol water | HCID 66602552 | — |
| Product | tert-butyl 6-(4-methylphenyl)-2H-1-benzopyran-3-carboxylate | HCID 10615821 | 74.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172061B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-508742d8bf7e45b8a757c618091e7d54 |
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| Source note | uspto-grants-2001_01 |
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