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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637676Generated: October 31, 2026

5-chloro-6-(piperidin-1-yl)-benzofuran-3(2H)-one → 5-Chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/637676

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-chloro-6-(piperidin-1-yl)-benzofuran-3(2H)-oneHCID 20255664—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventEthanolHCID 702—
Product5-Chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuranHCID 20255636—

Reaction Steps

200 mg of platinum oxide are added to a solution of 1.38 g (5.5 mmole) of 5-chloro-6-(piperidin-1-yl)-benzofuran-3(2H)-one in 20 ml of ethanol and the whole is hydrogenated at 3 atmospheres. The catalyst is filtered off and the filtrate is concentrated in a vacuum rotary evaporator. The residue is chromatographed over silica gel using methylene chloride as eluant. Recrystallisation from petroleum ether yields 5-chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuran having a melting point of 38°-40°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558043
Source datasetuspto-grants-1985_12
ORD IDord-1acbea09b980480ca2d8d59231e3c4db
Source noteuspto-grants-1985_12