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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384488Generated: November 1, 2026

Tetrahydrofuran → HCID 59526929, compound

https://huagongshe.com/reaction/384488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 59527482HCID 59527482—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 59526929HCID 5952692991.3%

Reaction Steps

To a mixture of benzyl 4-{(E)-2-[4-(benzyloxy)-3-methylquinolin-2-yl]vinyl}piperidine-1-carboxylate (978 mg), THF (6 mL) and ethanol (6 mL) was added 10% palladium-activated carbon (200 mg) under nitrogen atmosphere. The mixture was stirred at room temperature under hydrogen atmosphere of 3 atms, for 4 hours. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (Fuji Silysia Chemical Ltd., NH, eluent: chloroform/methanol=97/3˜92/8), and the solvent was evaporated. The residue was washed with ether, and collected by filtration to obtain 3-methyl-2-(2-piperidin-4-ylethyl)quinolin-4(1H)-one (490 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367702B2
Source datasetuspto-grants-2013_02
ORD IDord-0e31651bd28549f39fc64e84771c7f04
Source noteuspto-grants-2013_02