化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → 4-(2-Propenyl)-1,2,4-oxadiazolidine-3,5-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Hydroxyurethane | HCID 11510 | — |
| 反応物 | Allyl isocyanate | HCID 15123 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 4-(2-Propenyl)-1,2,4-oxadiazolidine-3,5-dione | HCID 22717680 | 158.9% |
反応手順
To a 500 mL round-bottom flask were added acetone (300 mL), allyl isocyanate (12.0 g, 0.145 mol), N-hydroxyurethane (6.1 g, 0.058 mol) and triethylamine (11.7 g, 0.116 mol) respectively at room temperature under nitrogen with efficient stirring. The reaction mixture was allowed to stir at room temperature for 6 d. The solvent was removed under reduced pressure. The residue was suspended in 100 mL of 1N HCl, extracted with ethyl acetate (3×150 mL). The organic solution was washed with water, brine, dried over MgSO4 and concentrated to a clear yellow oil. The crude product was dried under high vacuum for 4 h to give the title compound as an oil (13.1 g) which was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06737383B1 |
| 出典データセット | uspto-grants-2004_05 |
| ORD ID | ord-1c9694b018d84fe89c2602412811fbc3 |
| 出典メモ | uspto-grants-2004_05 |