化工社化工社 化学情報印刷レポート · 研究参考用
3-Chloro-2-chloromethyl-1-propene → Benzyl tert-butyl 4-methylidenepyrazolidine-1,2-dicarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Chloro-2-chloromethyl-1-propene | HCID 15859 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Benzyl tert-butyl hydrazine-1,2-dicarboxylate | HCID 11288582 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Benzyl tert-butyl 4-methylidenepyrazolidine-1,2-dicarboxylate | HCID 12970152 | — |
反応手順
To a suspension of NaH (3.81 g, 95.4 mmol) in DMF (80 mL) is add dropwise a solution of N-Cbz-N′-Boc-hydrazine (12.1 g, 45.4 mmol) in DMF (20 mL). The reaction mixture is stirred about 20 minutes and 3-chloro-2chloromethyl-propene (5.8 mL, 50 mmol) is added dropwise and the reaction is allowed to stir at room temperature until the reaction is complete by TLC, approximately 12 hours. The reaction solution is partitioned between ethyl acetate and water, the water layer being extracted several times more with solvent. The combined organic layers are dried, filtered, and concentrated to afford the desired product as a clear oil which is used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06849627B2 |
| 出典データセット | uspto-grants-2005_02 |
| ORD ID | ord-5ce49e33ff9e4d76b830e4eab483450a |
| 出典メモ | uspto-grants-2005_02 |