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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727208Generated: November 2, 2026

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

https://huagongshe.com/reaction/1727208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetyl-4-{[(4-chlorophenyl)methyl]oxy}piperidineHCID 69056298—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
Product4-{[(4-Chlorophenyl)methyl]oxy}piperidineHCID 1319442462.5%

Reaction Steps

1-acetyl-4-{[(4-chlorophenyl)methyl]oxy}piperidine (Preparation 99, 11 g, 41.1 mmol) in methanol (50 ml) and sodium hydroxide solution (5 M, 30 ml) were refluxed on a steam bath for 10 h. After cooling, methanol was removed and the remaining solution was extracted with petroleum ether (40-60, 3×30 ml). The organic extracts were dried (Na2SO4) and concentrated in vacuo to give an white solid (5.8 g, 62%). A portion was recrystallised from petroleum ether to give needle crystals (3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-fc942aec95c5456d88f45b261f17ecd3
Source noteuspto-grants-2009_02