HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-(5-Chloro-2-nitrophenyl)-1,3-dioxolane | HCID 267385 | — |
| Product | 2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolane | HCID 13987598 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04701459 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-780747b03da34d5da4302f7cf0abbebe |
| Source note | uspto-grants-1987_10 |