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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727209Generated: November 2, 2026

Water → 1-Acetyl-4-{[(4-chlorophenyl)methyl]oxy}piperidine

https://huagongshe.com/reaction/1727209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantSodium hydrideHCID 24758—
Reactant1-(4-Hydroxypiperidin-1-yl)ethan-1-oneHCID 10749291—
SolventDimethylformamideHCID 6228—
Product1-Acetyl-4-{[(4-chlorophenyl)methyl]oxy}piperidineHCID 6905629884.3%

Reaction Steps

1-Acetylpiperidin-4-ol (Preparation 193, 10 g, 70 mmol) in N,N-dimethylformamide (50 ml) was added dropwise to a stirred suspension of sodium hydride (50% wt dispersion in oil, 4.8 g, 0.1 mol) in N,N-dimethylformamide (50 ml) at room temperature under nitrogen. After stirring the reaction mixture for 3 hours, 4-chlorobenzyl chloride (12.8 g, 80 mmol) in N,N-dimethylformamide (50 ml) was added dropwise and the reaction mixture was stirred for a further 4 h. The solution was filtered and the filtrate was evaporated to give an orange oil. Water was added and the mixture was extracted with petroleum ether (3×50 ml) and then with diethyl ether (3×50 ml). The combined organic extracts were dried (Na2SO4) and concentrated to give the title compound as an orange oil (15.8 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-e6a512af005746f9970888d411622068
Source noteuspto-grants-2009_02