HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16780Erstellt: 25. Oktober 2026
Acetic Acid → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate
https://huagongshe.com/reaction/16780
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | (1-Ethoxycyclopropoxy)trimethylsilane | HCID 2734686 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | tert-Butyl 4-cyclopropylpiperazine-1-carboxylate | HCID 20294524 | 61,1% |
Reaktionsschritte
MeOH (0.3 mL), ((1-ethoxycyclopropyl)oxy)trimethylsilane (2 g, 11.47 mmol) and acetic acid (1.051 mL, 18.35 mmol) were added to a stirred solution of tert-butyl piperazine-1-carboxylate (1.068 g, 5.735 mmol) in THF (40 mL) under nitrogen. Sodium cyanoborohydride (0.541 g, 8.60 mmol) was added portionwise over a period of 10 mins. The resulting mixture was stirred at 60° C. for 24 h. The reaction mixture was evaporated to dryness and mixed with water (80 mL) and 1M HCl (25 mL). This solution was washed with EtOAc (2×50 mL), the aqueous layer was basified with K2CO3, and extracted with EtOAc (2×30 mL). The organic layers were combined, washed with saturated brine (30 mL), dried over MgSO4, filtered and evaporated to afford tert-butyl 4-cyclopropylpiperazine-1-carboxylate (0.792 g, 61.1%) as a colourless oil which crystallised on standing.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737149B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-4abb8072c06044d2986baf950fe93620 |
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| Quellennotiz | uspto-grants-2010_06 |
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