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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276155Generated: October 29, 2026

1,4-Dichlorobenzene → HCID 10130354, compound

https://huagongshe.com/reaction/276155

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DichlorobenzeneHCID 4685—
ReactantPiperidineHCID 8082—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10130354HCID 1013035459%

Reaction Steps

15 mmol of p-dichlorobenzene (2.2 g), 15.5 mmol of piperidine (1.3 g), 15.5 mmol of NaOEt solution in ethanol (10% by weight) and 50 mg of trans-di-μ-chlorobis[2-[bis(1,1-dimethylethyl)phosphino]-2-methylpropyl-C,P]dipallium(II) are suspended in 75 ml of dioxane and refluxed for 15 hours. After aqueous work-up, extraction with petroleum ether and drying over sodium sulfate, the solvents are removed under reduced pressure. This gives crude N-(4-chlorophenyl)piperidine as a light brown liquid which can be purified by distillation (boiling point: 50° C./0.08 torr); melting point: 69° C.; yield: 59%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353136B1
Source datasetuspto-grants-2002_03
ORD IDord-0a3d38878f2049c5851fcc6e859b79ed
Source noteuspto-grants-2002_03