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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645434Generated: November 1, 2026

1-Benzyl-4-piperidone → HCID 21918910, compound

https://huagongshe.com/reaction/645434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86591728HCID 86591728—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21918910HCID 21918910—

Reaction Steps

2.11 g (528 mmol) of 60% strength sodium hydride are initially charged in 50 ml of absolute tetrahydrofuran, and 15.7 g (52.8 mmol) of diethyl methanediphosphonate are added dropwise. The mixture is stirred at room temperature for another 30 minutes, and 10.1 g (52.8 mmol) of 1-benzyl-4-piperidone are then added. The mixture is stirred for one hour at room temperature and for one hour under reflux, concentrated, admixed with water and extracted three times with dichloromethane, and the organic phases are dried over sodium sulphate and concentrated. The residue is hydrogenated in 50 ml of ethanol over 1.7 g of 10% palladium-carbon at room temperature and 3 bar. The catalyst is filtered off with suction and the filtrate is concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704999B2
Source datasetuspto-grants-2010_04
ORD IDord-211f7f03657b458991b12d5b7fbee4a0
Source noteuspto-grants-2010_04