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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295807Generated: November 2, 2026

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

https://huagongshe.com/reaction/2295807

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 numberUS04426380
Source datasetuspto-grants-1984_01
ORD IDord-1fbb8ac5ee4d41e8a7925b3bc8ba8e5d
Source noteuspto-grants-1984_01