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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830246Generated: October 31, 2026

HCID 22054123, compound → HCID 22054317, compound

https://huagongshe.com/reaction/1830246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22054123HCID 22054123—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 22054317HCID 2205431793.3%

Reaction Steps

N-[5-(3,4,5,6-Tetramethoxy-2-methylbenzyl)-2-benzyloxybenzoyl]piperidine (1.02 g, 2.09 mmol) was dissolved in ethanol (50 ml) and the resulting solution was added to an ethanol suspension (5 ml) of 5% Pd—C (0.200 g) and stirred at room temperature for 16 hours in a hydrogen stream. The reaction solution was filtered, the filtrate was concentrated and the obtained residue was recrystallized from ether to obtain the titled compound (0.760 g, 1.95 mmol, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064124B2
Source datasetuspto-grants-2006_06
ORD IDord-d774d17bc12d45be9d80b61ad2373320
Source noteuspto-grants-2006_06