HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8744Erstellt: 23. Oktober 2026
1-Pentene, 5-bromo- → Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate
https://huagongshe.com/de/reaction/8744
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Pentene, 5-bromo- | HCID 70704 | — |
| Edukt | 1-N-Boc-4-Piperidinecarboxylic acid methyl ester | HCID 392870 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate | HCID 11232181 | 99,2% |
Reaktionsschritte
To a solution of potassium bis(trimethylsilyl)amide (30.7 g, 0.15 mol) in tetrahydrofuran (750 mL) at 0° C. was added a solution of methyl 1-(tert-butoxycarbonyl)piperidine-4-carboxylate (25 g, 0.10 mol) from Step A in tetrahydrofuran (250 mL) and the reaction mixture was stirred for 1 h. 5-Bromo-1-pentene (19.4 mL, 0.164 mol) was added and the reaction mixture was allowed to warm to room temperature for 1.5 h. The reaction mixture was then poured into saturated sodium bicarbonate solution and extracted three times with ethyl acetate. The organic layers were combined and washed with brine, dried over sodium sulfate, filtered, and concentrated to afford the title compound (30.9 g) which was used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07091211B2 |
|---|
| Quelldatensatz | uspto-grants-2006_08 |
|---|
| ORD ID | ord-292d55b0aa854c219dbd269febe9a838 |
|---|
| Quellennotiz | uspto-grants-2006_08 |
|---|