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Pyridine → N-(3,4-Dichlorophenyl)-N-methyl-3-oxobutanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Diketene | HCID 12661 | — |
| 反応物 | 3,4-Dichloro-N-methylaniline | HCID 2800931 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | N-(3,4-Dichlorophenyl)-N-methyl-3-oxobutanamide | HCID 13822492 | — |
反応手順
Dissolved in toluene were 3.5 g (0.02 mole) of 3,4-dichloro-N-methylaniline and a catalytic amount of pyridine, followed by a dropwise addition of 1.9 g (0.022 mole) of diketene at 50° C. After completion of the the dropwise addition, the resultant mixture was heated under reflux for 3 hours. The reaction mixture was cooled, and its organic layer was then washed with water, water, a 10% aqueous solution of hydrochloric acid and a 5% aqueous solution of sodium hydrogencarbonate in order. The thus-washed organic solution was dried nd concentrated to obtain 3',4'-dichloro-N-methylacetoacetoanilide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04910315 |
| 出典データセット | uspto-grants-1990_03 |
| ORD ID | ord-7c0465aa519b451481169f1ecd662385 |
| 出典メモ | uspto-grants-1990_03 |