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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663337Generated: October 29, 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/1663337

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 numberUS08034937B2
Source datasetuspto-grants-2011_10
ORD IDord-ebcabceb1ccd42958554a98d213b2cfc
Source noteuspto-grants-2011_10