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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230461Generated: October 29, 2026

Hydrochloric Acid → (RS)-2-{3-[1-(acenaphthen-1-yl)piperidin-4-yl]-2,3-dihydro-2-oxo-benzoimidazol-1-yl}acetic Acid

https://huagongshe.com/reaction/230461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl (RS)-2-{3-[1-(acenaphthen-1-yl)piperidin-4-yl]-2,3-dihydro-2-oxo-benzoimidazol-1-yl}acetateHCID 24900912—
SolventEthanolHCID 702—
Product(RS)-2-{3-[1-(acenaphthen-1-yl)piperidin-4-yl]-2,3-dihydro-2-oxo-benzoimidazol-1-yl}acetic AcidHCID 2306300286.6%

Reaction Steps

Ethyl (RS)-2-{3-[1-(acenaphthen-1-yl)piperidin-4-yl]-2,3-dihydro-2-oxo-benzoimidazol-1-yl}acetate (1.6 g) was dissolved in ethanol (10 ml) and 2N-aqueous sodium hydroxide solution (10 ml) was added. The mixture was stirred at room temperature for 30 min. The reaction mixture was poured into water, thereto was added to 1N-hydrochloric acid for neutralization, and the mixture was extracted with chloroform. The extract was washed with water and saturated brine, dried over magnesium sulfate, and concentrated. The obtained solid was washed with ethyl acetate to give the title compound (1.3 g) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566728B2
Source datasetuspto-grants-2009_07
ORD IDord-6cb4a7bb47f94c19a6318e570494283d
Source noteuspto-grants-2009_07