Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172225Generated: October 31, 2026

Ethanol → HCID 70873672, compound

https://huagongshe.com/reaction/2172225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 86709387HCID 86709387—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 70873672HCID 70873672—

Reaction Conditions

Temperature50 °C

Reaction Steps

Ethanol (20 ml) and ethyl acetate (10 ml) were added to 4-[4-(benzyloxy)benzylidene]-1-[4-(tetrahydro-2H-pyran-2-yloxy)phenyl]piperidine prepared in Reference Example 366. A palladium on carbon (0.378 g) was added to the mixture, and stirred at 50° C. for 4 hours under a hydrogen atmosphere. The insoluble matter was removed by filtration, and the filtrate was concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=6:1→4:1) to afford the title compound as a colorless amorphous compound (1.10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-fe318a0ae63841b4bc3b7fbc8505f5ee
Source noteuspto-grants-2015_06