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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488880Generated: October 30, 2026

Hydrochloric Acid → [7-Chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2h-chromen-3-yl]acetic acid

https://huagongshe.com/reaction/488880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl [7-chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2h-chromen-3-yl]acetate.hydrochlorideHCID 131725236—
SolventEthanolHCID 702—
Product[7-Chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2h-chromen-3-yl]acetic acidHCID 2226720596.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl [7-chloro-2-oxo-4-phenyl-6-[(4-phenylpiperazin-1-yl)methyl]-2H-chromen-3-yl]acetate.hydrochloride (40 g) was suspended in ethanol (120 ml), and combined with a 2 N aqueous solution of sodium hydroxide (144.5 ml). A yellow clear solution obtained by stirring at 70° C. for 1 hour was added dropwise to a mixture solution of ethanol (40 ml) and 6 N hydrochloric acid (49.4 ml) over 45 minutes. The reaction solution was adjusted to pH 5.5 to 6.0 with sodium hydrogen carbonate at 40° C. After pH became stable, the mixture was stirred at 35 to 40° C. internal temperature for 15 minutes, and cooled to room temperature, and stirred at room temperature for 30 minutes. The crystal formed was filtered and washed with 30% ethanol to obtain the title compound (34 g, yield: 96%) as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974806B2
Source datasetuspto-grants-2005_12
ORD IDord-904ee024d0f248b78f0653a1e239daa3
Source noteuspto-grants-2005_12