Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Pentane | HCID 8003 | — |
| Edukt | 1-Aminopiperidine | HCID 16658 | — |
| Edukt | N-(2-chloroethyl)-N-nitrosocarbamoylazide | HCID 10654895 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 86738825 | HCID 86738825 | 21% |
Reaktionsschritte
To a solution of 0.1 mole N-(2-chloroethyl)-N-nitrosocarbamoylazide in 75 ml dichloromethane is added in drops at -5 degC. (°C.) under stirring within 2 hours a solution of 0.2 mole N-aminopiperidine in 20 ml of a mixture of 4 parts by volume dichloromethane and 1 part by volume n-pentane. After the addition, the stirring is continued for one hour and a whitish-yellow precipitate is obtained. Subsequently it is shaken out with the same volume of 0.1 N H2SO4. The organic phase is dried over Na2SO4 and concentrated on the rotary evaporator. From ethyl formate/n-pentane we obtain on standing in the deep freezer yellow crystals which are homogeneous in thin-layer chromatography, after recrystallization from the same solvent mixture (silicagel foils, solvent system n-pentane/diethylether/dichloromethane 5:2:2)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04377687 |
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| Quelldatensatz | uspto-grants-1983_03 |
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| ORD ID | ord-e453c6e61c9b4fa3a7ff75464caa5402 |
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| Quellennotiz | uspto-grants-1983_03 |
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