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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256179Generated: October 26, 2026

Piperidine → 2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolane

https://huagongshe.com/reaction/256179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-(5-Chloro-2-nitrophenyl)-1,3-dioxolaneHCID 267385—
Product2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolaneHCID 13987598100%

Reaction Steps

A mixture of 2-(5-chloro-2-nitrophenyl)-1,3-dioxolane (21.3 g, 0.09 mole) and piperidine (39.6 g, 0.46 mole) was heated at reflux in an oil bath. After 3 hours, excess piperidine was evaporated and the residue partitioned between water and dichloromethane. The organic phase was separated and the aqueous layer extracted with dichloromethane. Combined extracts were washed with water, dried over magnesium sulfate and concentrated in vacuo to afford 2-(2-nitro-5-piperdinylphenyl)-1,3-dioxolane (21.6 g, 100%) as a dark colored oil which was used without further purification. An analytical sample was purified by flash chromatography using dichloromethane as eluant to give a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04701459
Source datasetuspto-grants-1987_10
ORD IDord-780747b03da34d5da4302f7cf0abbebe
Source noteuspto-grants-1987_10