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Sulfuric Acid → trimethylpyruvic acid N-acetylamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | 3,3-Dimethyl-2-oxobutanenitrile | HCID 94527 | — |
| 生成物 | trimethylpyruvic acid N-acetylamide | HCID 12769196 | 86.5% |
反応手順
Firstly 25.6 g (0.25 mol) of acetic anhydride and then 27.8 g (0.25 mol) of pivaloyl cyanide were introduced, in each case at room temperature, into 49.0 g (0.5 mol) of initially introduced concentrated sulphuric acid. After the reaction mixture had been further stirred for 4 hours, 150 g of ice-water were added to it and it was thoroughly stirred. The precipitated reaction product was filtered off under suction, washed with 100 ml of water and dried. 37.0 g (86.5% of theory) of trimethylpyruvic acid N-acetylamide were obtained as colorless shiny platelets of melting point 82° to 84° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04408044 |
| 出典データセット | uspto-grants-1983_10 |
| ORD ID | ord-9e02003dfc9a44e48206f8ccd084de93 |
| 出典メモ | uspto-grants-1983_10 |