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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216029Generated: October 29, 2026

1,4-Dioxane → 4-allyl-N-(3-chlorophenyl)piperidine-4-carboxamide

https://huagongshe.com/reaction/216029

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantTert-butyl 4-allyl-4-(3-chlorophenylcarbamoyl)piperidine-1-carboxylateHCID 67036827—
SolventMethanolHCID 887—
Product4-allyl-N-(3-chlorophenyl)piperidine-4-carboxamideHCID 68991112—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl 4-allyl-4-(3-chlorophenylcarbamoyl)piperidine-1-carboxylate from step A (0.172 g, 0.453 mmol) in MeOH (10 mL) was added 4 MHCl in dioxane (0.340 mL, 1.36 mmol). The reaction was heated at 50° C. for 30 min, and then concentrated under vacuum, re-dissolved in MeOH and re-concentrated twice to give the title compound as the hydrochloride salt. MS (ES+) [M+H]+=279.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193202B2
Source datasetuspto-grants-2012_06
ORD IDord-6498dcf92aa943d1b591ff9b658bcf7e
Source noteuspto-grants-2012_06