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Water → 1-(4-Nitrobenzyl)pyrrolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Pyrrolidine | HCID 31268 | — |
| 反応物 | 4-Nitrobenzyl bromide | HCID 66011 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(4-Nitrobenzyl)pyrrolidine | HCID 783522 | — |
反応手順
In THF (250 ml) was dissolved 4-nitrobenzyl bromide (25.0 g), and to the mixture was added pyrrolidine (24.1 ml) at 0° C. The reaction mixture was stirred at room temperature for 60 hours. To the mixture was added water (500 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate) to give 1-(4-nitrobenzyl)pyrrolidine (23.5 g) as orange oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06172061B2 |
| 出典データセット | uspto-grants-2001_01 |
| ORD ID | ord-06eaee2ca1cf4793a41eef3f46cd71f5 |
| 出典メモ | uspto-grants-2001_01 |