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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488865Generated: October 30, 2026

Water → ethyl(7-chloro-6-methyl-2-oxo-4-phenyl-2H-chromen-3-yl)acetate

https://huagongshe.com/reaction/488865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant(4-Chloro-2-hydroxy-5-methylphenyl)(phenyl)methanoneHCID 9992150—
Reactant2-Ethylbutanedioyl dichlorideHCID 21864608—
SolventTetrahydrofuranHCID 8028—
Productethyl(7-chloro-6-methyl-2-oxo-4-phenyl-2H-chromen-3-yl)acetateHCID 2226725753%

Reaction Steps

A solution of (4-chloro-2-hydroxy-5-methylphenyl)(phenyl)methanone (5.0 g) and triethylamine (5.65 ml) in THF (100 ml) was combined with ethyl succinyl chloride (3.47 ml) at 0° C., and stirred for 1 hour. The reaction solution was combined with water, and the product was extracted with ethyl acetate. The extract was washed with a 1 N solution of hydrochloric acid followed by a saturated aqueous solution of sodium chloride, and after drying over magnesium sulfate, the solvent was distilled off under reduced pressure. The resultant residue was dissolved in toluene (50 ml), combined with DBU (1.25 ml), and heated under reflux for 2.5 hours. After cooling, the reaction solution was diluted with ethyl acetate (100 ml), and washed with water followed by a 1 N solution of hydrochloric acid and a saturated aqueous solution of sodium chloride. After drying over magnesium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by a column chromatography (packing: silica gel, eluent: ethyl acetate-hexane=1:4) and further purified by recrystallization from ethyl acetate-hexane to obtain the title compound (3.86 g, yield: 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974806B2
Source datasetuspto-grants-2005_12
ORD IDord-b0f0c539b11549e18327e4d06625831b
Source noteuspto-grants-2005_12