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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666962Generated: October 31, 2026

1'-Benzyl-1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine] → 1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine]

https://huagongshe.com/reaction/1666962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1'-Benzyl-1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine]HCID 59756816—
CatalystPalladiumHCID 23938—
Solvent2,2,2-TrifluoroethanolHCID 6409—
Product1H-spiro[furo[3,4-c]pyridine-3,4'-piperidine]HCID 46735163107.8%

Reaction Steps

A solution of 0.22 g (0.78 mmol) 1′-benzyl-1H-spiro[furo[3,4-c]pyridine-3,4′-piperidine] in 8 ml 2,2,2-trifluoroethanol was purged with argon prior to adding 0.08 g (10 mol %) palladium on activated charcoal. The flask was evacuated, refilled with hydrogen gas and stirred under an atmosphere of hydrogen gas for 20 h. The catalyst was filtered off and washed with ethanol. The filtrate was concentrated to dryness to give the title compound (0.16 g, quantitative, purity of approximately 95%) as a light yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044202B2
Source datasetuspto-grants-2011_10
ORD IDord-0818a89a049c40228ff42f59c9751872
Source noteuspto-grants-2011_10