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Dimethylformamide → 2-(4-Hydroxy-3-methoxy-5-nitrobenzoyl)-3-methylindole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Phenacylamine | HCID 11952 | — |
| 反応物 | 2-Bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone | HCID 14450983 | — |
| 生成物 | 2-(4-Hydroxy-3-methoxy-5-nitrobenzoyl)-3-methylindole | HCID 21458979 | — |
反応手順
ac) A solution of 29.0 g of 2-bromo-4'-hydroxy-3'-methoxy-5'-nitroacetophenone and 13.5 g of 2-aminoacetophenone in 250 ml of dry N,N-dimethylformamide is stirred at 90° for 16 hours. The reaction mixture is then evaporated to about two thirds and poured on to ice. The separated crystals are filtered under suction and dissolved in methylene chloride. The solution is washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. There is obtained 2-(4-hydroxy-3-methoxy-5-nitrobenzoyl)-3-methylindole of m.p. 195°-197° (from methylene chloride/methanol).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05389653 |
| 出典データセット | uspto-grants-1995_02 |
| ORD ID | ord-9b3c989b9113448f9692f78581fca85a |
| 出典メモ | uspto-grants-1995_02 |