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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637684Generated: October 31, 2026

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

https://huagongshe.com/reaction/637684

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-hydroxy-6-(piperidin-1-yl)-2,3-dihydrobenzofuranHCID 20255634—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventEthanolHCID 702—
Product5-Chloro-6-(piperidin-1-yl)-2,3-dihydrobenzofuranHCID 20255636—

Reaction Steps

5 mg of platinum oxide are added to a solution of 250 mg (1.00 mmole) of crude 5-chloro-2-hydroxy-6-(piperidin-1-yl)-2,3-dihydrobenzofuran in 5 ml of absolute ethanol and the whole is hydrogenated at room temperature and 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-1c1b54bbe5ea42f68d170fbcc0f906ad
Source noteuspto-grants-1985_12