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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666959Generated: November 1, 2026

1'-Benzyl-5H-spiro[furo[3,4-b]pyridine-7,4'-piperidine] → 5H-Spiro[furo[3,4-b]pyridine-7,4'-piperidine]

https://huagongshe.com/reaction/1666959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1'-Benzyl-5H-spiro[furo[3,4-b]pyridine-7,4'-piperidine]HCID 59756819—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5H-Spiro[furo[3,4-b]pyridine-7,4'-piperidine]HCID 5975682491%

Reaction Steps

A solution of 0.39 g (1.4 mmol) 1′-benzyl-5H-spiro[furo[3,4-b]pyridine-7,4′-piperidine] in 14 ml ethanol was purged with argon prior to adding 0.15 g (10 mol %) palladium on activated charcoal. The flask was evacuated, refilled with hydrogen gas and stirred at room temperature under an atmosphere of hydrogen for 16 h. The catalyst was filtered off and washed with ethanol. The filtrate was concentrated to dryness to give the title compound (0.24 g, 91%) as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044202B2
Source datasetuspto-grants-2011_10
ORD IDord-fe8dd7df1feb4faeb96a29a59f3aac47
Source noteuspto-grants-2011_10