HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8748Erstellt: 25. Oktober 2026
Ethyl Acetate → 8-tert-Butyl 2-methyl 1-oxo-8-azaspiro[4.5]decane-2,8-dicarboxylate
https://huagongshe.com/reaction/8748
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| Edukt | Methyl 4-(1-(tert-butoxycarbonyl)-4-(methoxycarbonyl)piperidin-4-yl)butanoate | HCID 69183850 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 8-tert-Butyl 2-methyl 1-oxo-8-azaspiro[4.5]decane-2,8-dicarboxylate | HCID 21983897 | 110,2% |
Reaktionsschritte
To a solution of methyl 4-(1-(tert-butoxycarbonyl)-4-(methoxycarbonyl)piperidin-4-yl)butanoate (20.1 g, 0.058 mol) from Step E in tetrahydrofuran (600 mL) at −78° C. was added lithium diisopropylamide mono(tetrahydrofuran) (47 mL, 0.070 mol, 1.5M solution in cyclohexanes). The reaction mixture was stirred at −78° C. for 25 min. Thin layer chromatography (tlc) analysis (50% ethyl acetate in hexanes) showed that starting material remained. Additional lithium diisopropylamide mono(tetrahydrofuran) (31 mL) was added and the reaction mixture was stirred for 20 min. The reaction mixture was poured into saturated ammonium chloride and extracted three times with diethyl ether. The organic layers were combined, washed with brine, dried over sodium sulfate, and concentrated to afford the title compound (19.9 g) which was taken on to the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091211B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-2199290325e045e6997c103221fdd023 |
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| Quellennotiz | uspto-grants-2006_08 |
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