Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | Ethyl 4-bromo-2-methylbutanoate | HCID 12780980 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | Ethyl 2-methyl-4-piperidinobutyrate | HCID 20361120 | — |
Reaktionsschritte
10.5 g. (0.05 mole) of ethyl γ-bromo-α-methylbutyrate was combined with 17.0 g. (0.20 mole) of piperidine and 100 ml. of benzene and stirred for 16 hours at room temperature and heated at 60° C. for 4 hours. The reaction mixture was cooled and the colorless solid which appeared was removed by filtration. The mother liquor was concentrated to give ethyl α-methyl-γ-piperidinobutyrate as a mobile yellow liquid which distilled (b.p. 78° C. at 0.25 mm.) as 6.7 g. (63%) of colorless liquid. The nuclear magnetic resonance and infrared spectra were consistent with the desired compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04042694 |
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| Quelldatensatz | uspto-grants-1977_08 |
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| ORD ID | ord-5285d10f4538403f9ea38ebefec88d98 |
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| Quellennotiz | uspto-grants-1977_08 |
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