HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1942215Erstellt: 25. Oktober 2026
Hydrochloric Acid → 2-(4-Cyclopropyl-phenyl)-2,8-diaza-spiro[4.5]decan-1-one
https://huagongshe.com/reaction/1942215
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 4-Cyclopropylaniline | HCID 12253927 | — |
| Edukt | Dimethylalumanylium chloride | HCID 16686359 | — |
| Edukt | 4-(2-Methoxy-ethyl)-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester | HCID 58287261 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-(4-Cyclopropyl-phenyl)-2,8-diaza-spiro[4.5]decan-1-one | HCID 58287277 | — |
Reaktionsschritte
A mixture of 1.3 g (4.1 mmol) 4-(2-Methoxy-ethyl)-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester, 0.604 g (4.5 mmol) 4-cyclopropylaniline and 8.24 mL (8.24 mmol) dimethylaluminum chloride (1N in hexane) in 100 mL toluene was stirred at 115° C. for 15 h. After cooling to room temperature the mixture was poured into ice, the mixture was acidified with HCl aq. to pH=2 and extracted with ethyl acetate. The aqueous layer was basified with NaOH pellets to pH=8 and extracted with DCM. The combined organic layers were dried with MgSO4 and evaporated to dryness. The residue was purified by column chromatography on silica (amine) with a gradient formed from ethyl acetate and methanol to yield after evaporation of the product containing fractions 0.468 g (42%) of the title compound as light yellow solid. MS m/e: 270.0 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08389539B2 |
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| Quelldatensatz | uspto-grants-2013_03 |
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| ORD ID | ord-f0b6a5a0714b42829f5416cad43f52cd |
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| Quellennotiz | uspto-grants-2013_03 |
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