Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Benzhydrylpiperidine | HCID 88278 | — |
| Edukt | HCID 12796194 | HCID 12796194 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Produkt | HCID 12796197 | HCID 12796197 | 149,6% |
Reaktionsschritte
To a solution of 9.75 grams (26.39 millimoles) of 6-(3,5-dioxomorpholino)hexyl p-toluenesulfonate (prepared as described in Example IX) in 160 milliliters of warm tertiary butyl alcohol was added portionwise at temperatures in the range of 30°-32° C. over a period of about 23 minutes, 63 grams (26.38 millimoles) of 4-benzhydrylpiperidine in 160 milliliters of tertiary-butyl alcohol. The reaction mixture was heated at reflux temperature for about 22 hours and thereafter the solvent removed by vaporization to obtain 17.7 grams of a 4-[6-(4-benzhydrylpiperidino)hexyl]-3,5-dioxomorpholine product as a yellow oil. Crystallization (twice) from ethyl acetate produced 4.19 grams of white crystals, m.p., 121°-124.5° C. and having NMR, UV and IR spectral characteristics appropriate for the product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04256891 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-555f25c28eb04998b04b819d870496e5 |
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| Quellennotiz | uspto-grants-1981_03 |
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