HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1530649Erstellt: 27. Oktober 2026
Methanol → Tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate
https://huagongshe.com/reaction/1530649
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methanol | HCID 887 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Diisobutylaluminum hydride | HCID 14487 | — |
| Edukt | Tert-butyl 2-(1-methylpiperidin-4-ylidene)hydrazinecarboxylate | HCID 21097379 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate | HCID 68313226 | 69,4% |
Reaktionsschritte
To a solution of tert-butyl 2-(1-methylpiperidin-4-ylidene)hydrazinecarboxylate (500 mg, 2.20 mmol) in THF (50 mL) was added DIBAl-H (22 mL, 22 mmol) under nitrogen atmosphere. The resulting mixture was stirred at 25° C. overnight. Methanol (5 mL) was added to quench the reaction at −78° C. After being stirred at room temperature for 1 h, water (10 mL) was added. The solid was filtered off and washed with EtOAc. The combined filtrate was partitioned and extracted with EtOAc (3×50 mL), dried over Na2SO4, and concentrated. The residue was purified by silica gel chromatography eluting with EtOAc/petroleum ether (1:10) to give tert-butyl 2-(1-methylpiperidin-4-yl)hydrazinecarboxylate (350 mg, 69% yield) as a colorless oil. LCMS (ESI) m/z: 230.4 [M+H+].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09090628B2 |
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| Quelldatensatz | uspto-grants-2015_07 |
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| ORD ID | ord-85c9a7c1b86540e0a58e0307bac4a0ed |
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| Quellennotiz | uspto-grants-2015_07 |
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