HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Chloro-2-chloromethyl-1-propene → Benzyl tert-butyl 4-methylidenepyrazolidine-1,2-dicarboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Chloro-2-chloromethyl-1-propene | HCID 15859 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Benzyl tert-butyl hydrazine-1,2-dicarboxylate | HCID 11288582 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Benzyl tert-butyl 4-methylidenepyrazolidine-1,2-dicarboxylate | HCID 12970152 | — |
Reaktionsschritte
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-2-chloromethyl-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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07087615B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-16ce0de6403640198e3f969730ca292f |
| Quellennotiz | uspto-grants-2006_08 |