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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091792Generated: November 2, 2026

Hydrochloric Acid → 1-[(Piperidin-4-yloxy)acetyl]piperidine

https://huagongshe.com/reaction/1091792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl 4-(2-oxo-2-(piperidin-1-yl)ethoxy)piperidine-1-carboxylateHCID 57791806—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product1-[(Piperidin-4-yloxy)acetyl]piperidineHCID 24208838—

Reaction Steps

A 4 N HCl solution in dioxane (6 mL) was added to a solution of tert-butyl 4-(2-oxo-2-(piperidin-1-yl)ethoxy)piperidine-1-carboxylate (111) (7.5 g, 22.98 mmol) in MeOH (20 mL) and the reaction mixture was stirred at room temperature for 6 hours. Removal of solvent afforded 1-(piperidin-1-yl)-2-(piperidin-4-yloxy)ethanone as its hydrochloride salt (2.300 g, 44.2%). This salt was then dissolved in methanol (50 ml) and MP-carbonate (14.88 g, 33.61 mmol) was added. The resulting mixture was filtered and the solvent removed to give the desired compound (2.300 g, 44.2%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129380B2
Source datasetuspto-grants-2012_03
ORD IDord-3b9f0a5f739846a095556e11c5c3a677
Source noteuspto-grants-2012_03