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Acetonitrile → N-(Triphenylmethyl)piperazine-2,3-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Trityl chloride | HCID 6456 | — |
| 反応物 | 2,3-Piperazinedione | HCID 72761 | — |
| 反応物 | Bistrimethylsilylacetamid | HCID 11708267 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(Triphenylmethyl)piperazine-2,3-dione | HCID 14182487 | 89.4% |
反応手順
A mixture of 2,3-piperazinedione (11.4 g, 100 mmol), bistrimethylsilylacetamide (55.7 g, 270 mmol) and 150 ml of acetonitrile was heated under reflux for one hour. Within 30 minutes, triphenylmethylchloride (22.2 g, 80 mmol) was added dropwise and the mixture was again refluxed for two hours. After stirring overnight at room temperature, 21.6 ml of water was added to the clear solution. The resulting precipitate (3.13 g) was filtered off and the filtrate concentrated in vacuo. The residue was triturated with water and dried to yield 25.5 g of crude title compound which was recrystallized from ethanol. Yield of pure product: 12.19 g, melting point 230°-235° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04743685 |
| 出典データセット | uspto-grants-1988_05 |
| ORD ID | ord-8cf77d2a956840f18aa254d0f1397d22 |
| 出典メモ | uspto-grants-1988_05 |