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Pyridine → N-(2-Bromoethyl)-p-nitrobenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| 反応物 | 2-Bromoethylamine hydrobromide | HCID 2774217 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | N-(2-Bromoethyl)-p-nitrobenzamide | HCID 458985 | — |
反応手順
In 30 ml of chloroform were added 3 g of 4-nitrobenzoyl chloride, 3.3 g of 2-aminoethyl bromide hydrobromide and 3.9 ml of pyridine under ice cooling, and they were stirred at the same temperature for 1 hour. The reaction mixture was then washed with water, and the resulting organic layer was concentrated to obtain a crude product of 2-(4-nitrobenzoylamino)ethyl bromide. Afterward, the latter was recrystallized from hexane/ethanol, the resulting crystals were collected by filtration, washed and dried to prepare 2.9 g of 2-(4-nitrobenzoylamino)ethyl bromide (compound 46).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05008267 |
| 出典データセット | uspto-grants-1991_04 |
| ORD ID | ord-6552b384b67f4658950798dd857919fd |
| 出典メモ | uspto-grants-1991_04 |