化工社化工社 化学情報印刷レポート · 研究参考用
Dimethadione → 2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethadione | HCID 3081 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-[3-(1-Adamantyl)-2-chloro-3-oxopropanamido]-4-nitroanisole | HCID 19347758 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-[3-(1-Adamantyl)-2-(5,5-dimethyl-2,4-dioxooxazolidinyl)-3-oxopropanamido]-4-nitroanisole | HCID 53879666 | 79.8% |
反応手順
A suspension of 16.28 g (0.04 mol) of [4], 5.17 g (0.04 mol) of 5,5-dimethyloxazolidine-2,4-dione, and 16.58 g (0.12) mol of anhydrous potassium carbonate in 380 mL of dried acetone was refluxed for 3 hours. Thin layer chromatographic analysis indicated that the reaction was complete. The reaction mixture was concentrated in vacuo to yield an orange-colored solid. It was dissolved in ethyl acetate and the organic layer was washed with HCl (10%) and brine until neutrality. The organic layer was dried, filtered, and concentrated to yield an oil which solidified upon standing. It was triturated in ligroin. The final dried product (15.92 g, 79.8%) gave one spot on TLC. All analytical data confirmed the assigned structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06040126 |
| 出典データセット | uspto-grants-2000_03 |
| ORD ID | ord-8147e9c6089444d39b250676fc062f57 |
| 出典メモ | uspto-grants-2000_03 |