Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Azide | HCID 33557 | — |
| Edukt | 2,2-Diphenyl-4-(4-phenylpiperidino)butyronitrile | HCID 21404797 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ammonium Chloride | HCID 25517 | — |
| Lösungsmittel | Lithium Chloride | HCID 433294 | — |
| Produkt | HCID 178420099 | HCID 178420099 | — |
Reaktionsschritte
11.0 Parts of 2,2-diphenyl-4-(4-phenylpiperidino)butyronitrile are dissolved in 55 parts by volume of dimethylformamide along with 2.82 parts of sodium azide, 2.32 parts of ammonium chloride and 0.04 parts of lithium chloride. This mixture is heated under a nitrogen atmosphere, in an oil bath which is kept at 125° C. The solution is cooled and poured into water which caused the formation of a gummy precipitate. The solvent phase is decanted from the gum. The gum is then crystallized from a mixture of methanol-ether and dried in vacuum to provide an off-white solid which is recrystallized from a mixture of methanol-ether and again dried in vacuum to provide 5-[1,1-diphenyl-3-(4-phenylpiperidino)propyl]-1H-tetrazole hemimethanolate, melting at 149° - 157° C. and having the following formula ##STR8##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04053477 |
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| Quelldatensatz | uspto-grants-1977_10 |
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| ORD ID | ord-b5779c0e6f5340a0a8606def85790994 |
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| Quellennotiz | uspto-grants-1977_10 |
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