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Piperidine → 2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 2-(5-Chloro-2-nitrophenyl)-1,3-dioxolane | HCID 267385 | — |
| 生成物 | 2-(2-Nitro-5-piperdinylphenyl)-1,3-dioxolane | HCID 13987598 | 100% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04701459 |
| 出典データセット | uspto-grants-1987_10 |
| ORD ID | ord-780747b03da34d5da4302f7cf0abbebe |
| 出典メモ | uspto-grants-1987_10 |