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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790475Generated: November 3, 2026

Ethyl Acetate → HCID 22038394, compound

https://huagongshe.com/reaction/1790475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantChlorosuccinimideHCID 31398—
Reactant214616-13-4HCID 22038165—
SolventDichloromethaneHCID 6344—
ProductHCID 22038394HCID 2203839421%

Reaction Steps

N-Chlorosuccinimide (0.15 g) was added at room temperature to a solution of 1-[1-(4-fluorophenethyl)piperidin-4-yl]-6-methoxyindoline (0.39 g) in methylene chloride (5 ml) and the resultant mixture was stirred for 20 min. Then a 5 N aqueous solution of sodium hydroxide and ethyl acetate were added to the reaction solution and the layers were separated. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The resulting residue was purified by silica gel column chromatography (methylene chloride/ethanol system) followed by conversion into a hydrochloride to give the hydrochloride (0.10 g) of the title compound as apale red powder (yield: 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-918ca2d6d59f4de195adab010f5988c0
Source noteuspto-grants-2006_07