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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085343Generated: November 1, 2026

Ethanol → HCID 22282577, compound

https://huagongshe.com/reaction/2085343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 22282626HCID 22282626—
CatalystHCID 178418397HCID 178418397—
ProductHCID 22282577HCID 2228257799%

Reaction Steps

4-[(trifluoromethyl)sulfonyl]-2H-chromene from reaction 34a (1.78 g, 6.47 mmol) and 4-(methoxy carbonylphenyl) boronic acid (1.0 g, 5.6 mmol) were dissolved in ethanol (15 mL) and toluene (30 mL) under nitrogen at room temperature. Then lithium chloride (0.52 g, 12.35 mmol) and 2.65 M potassium carbonate (4.2 mL, 11.0 mmol) were added. Nitrogen was bubbled through the reaction for 15 minutes before the tetrakis(triphenylphosphine)palladium(0) (0.35 g, 0.31 mmol) was added. The reaction was heated to reflux for 3 h, allowed to cool then partitioned between ethyl acetate and water. The organic layer was washed with water, brine, dried over magnesium sulfate, and was concentrated. The product was purified by chromatography on silica gel eluting with ethyl ether:hexane (20:80, v:v) to give methyl 4-(2H-chromen-4-yl)benzoate (1.53 g, 99%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720329B2
Source datasetuspto-grants-2004_04
ORD IDord-dcb3f6d973df4b319f6a74c6d1a21266
Source noteuspto-grants-2004_04