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Tetrahydrofuran → 1-(N-(5,5,7,7-tetramethyl-2-octenyl)-2-aminoethyl)piperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Aminoethylpiperazine | HCID 8795 | — |
| 反応物 | 1-Chloro-5,5,7,7-tetramethyl-2-octene | HCID 135970 | — |
| 反応物 | Magnesium monoxide | HCID 6850729 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1-(N-(5,5,7,7-tetramethyl-2-octenyl)-2-aminoethyl)piperazine | HCID 54279970 | — |
反応手順
In a similar manner to Example 4, 10 g (4.95 mmol) of 1-chloro-5,5,7,7-tetramethyl-2-octene, 64 g (495 mmol) of 1-(2-aminoethyl)piperazine, 10 g (248 mmol) of magnesium oxide and 30 ml of THF are refluxed for 4 h. The mixture is diluted with 300 ml of diethyl ether and extracted once each with 5% strength aqueous NaOH and water, concentrated and dried at 40° C./1 mbar. Yield: quantitative.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05332791 |
| 出典データセット | uspto-grants-1994_07 |
| ORD ID | ord-f9768a04c5f04233933fd3961f83c583 |
| 出典メモ | uspto-grants-1994_07 |