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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190903Generated: October 31, 2026

Hydrochloric Acid → 4-Hydroxy-6-(4-methoxy-phenyl)-2-oxo-2H-chromene-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/2190903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant4-Methoxyphenyl boric acidHCID 14769994—
Reactant6-bromo-4-hydroxy-2-oxo-2H-chromene-3-carboxylic acid methyl esterHCID 86649459—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Hydroxy-6-(4-methoxy-phenyl)-2-oxo-2H-chromene-3-carboxylic acid methyl esterHCID 8664945868.6%

Reaction Steps

To a mixture of 6-bromo-4-hydroxy-2-oxo-2H-chromene-3-carboxylic acid methyl ester (150 mg, 0.5 mmol; example 2-b) in dimethoxyethane (DME) was added 4-methoxyphenylboroic acid (92 mg, 0.6 mmol), tetrakis(triphenylphosphine)palladium(0) (58 mg, 0.05 mmol) and 2N aq Na2CO3 (0.62 mL). The resulting mixture was purged with N2 for 1 min and heated to reflux for 2 h. Reaction mixture was diluted with water (50 mL) and acidified by 1 N aq HCl to pH=3-4. Precipitate was collected and dissolved in EtOAc. Insoluble was filtered off and the filtrate was dried over MgSO4, filtered, and concentrated. The crude product was triturated with MeOH (10 mL) and filtered. Resulting solid was dried in vacuo to give the title compound (112 mg). MS ESI(+) m/e: 327 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324405B2
Source datasetuspto-grants-2012_12
ORD IDord-e340b7bb8eef41139c0127027928d318
Source noteuspto-grants-2012_12