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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637678Generated: October 31, 2026

5-Chloro-3-hydroxy-6-(piperidin-1-yl)-2,3-dihydrobenzofuran → 5-Chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuran

https://huagongshe.com/reaction/637678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-3-hydroxy-6-(piperidin-1-yl)-2,3-dihydrobenzofuranHCID 20255650—
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 1.42 g (5.60 mmole) of 5-chloro-3-hydroxy-6-(piperidin-1-yl)-2,3-dihydrobenzofuran 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-d2448b89adee4b35aa4146dacce94c01
Source noteuspto-grants-1985_12