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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544714Generated: October 30, 2026

Dicyclohexylcarbodiimide → 5-chloro-6-(piperidin-1-yl)-benzofuran-2(3H)-one

https://huagongshe.com/reaction/544714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant5-Chloro-2-hydroxy-4-(piperidin-1-yl)-phenylacetic acidHCID 53913044—
SolventDichloromethaneHCID 6344—
Product5-chloro-6-(piperidin-1-yl)-benzofuran-2(3H)-oneHCID 13576952—

Reaction Steps

A solution of 6.5 g (31.5 mmoles) of dicyclohexylcarbodiimide in 40 ml of absolute methylene chloride is added at room temperature in the course of approximately 3 minutes to a solution of 8.1 g (30 mmoles) of crude 5-chloro-2-hydroxy-4-(piperidin-1-yl)-phenylacetic acid in 50 ml of absolute methylene chloride. The reaction mixture is stirred at room temperature for 30 minutes. The precipitated dicyclohexylurea is filtered off with suction and washed with methylene chloride. The filtrate is concentrated by evaporation in a vacuum rotary evaporator and the residue is chromatographed over silica gel with the eluant methylene chloride/hexane (1:1). Recrystallisation from hexane yields 5-chloro-6-(piperidin-1-yl)-benzofuran-2(3H)-one having a melting point of 129°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04451462
Source datasetuspto-grants-1984_05
ORD IDord-651c7a7cd4f84285988f9a7cb5b05936
Source noteuspto-grants-1984_05