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Acetic Acid → 1-(2-nitrobenzyl)-1H-pyrrole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | 2,5-Dimethoxytetrahydrofuran | HCID 79098 | — |
| 反応物 | (2-Nitrophenyl)methanamine | HCID 423893 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-(2-nitrobenzyl)-1H-pyrrole | HCID 12837707 | — |
反応手順
The starting material is prepared as follows: The mixture of 3,078 g of o-nitrobenzylamine and 2,670 g of 2,5-dimethoxytetrahydrofuran is added rapidly to 10,000 ml of glacial acetic acid at 86° while stirring under nitrogen. The mixture is stirred at 95° for 1.25 hours, cooled to 25° and combined with 30,000 ml of water. It is extracted with ethyl acetate, the extract is washed with 10% aqueous sodium hydroxide and 10% aqueous sodium chloride, filtered and evaporated to yield the 1-(o-nitrobenzyl)-pyrrole.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04316900 |
| 出典データセット | uspto-grants-1982_02 |
| ORD ID | ord-e992fb8e8999490195b0aaaf80f95508 |
| 出典メモ | uspto-grants-1982_02 |