4-Chlorobutyronitrile → HCID 178478461, Verbindung
Reaktionsgleichung
[Cl:1][CH2:2][CH2:3][CH2:4][C:5]#[N:6].[N-:7]=[N+:8]=[N-:9].[Na+].[Cl-].[NH4+].[OH-].[Na+]>CN(C)C=O>[Cl:1][CH2:2][CH2:3][CH2:4][C:5]1[NH:9][N:8]=[N:7][N:6]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 140 °C
Versuchsvorschrift
A mixture of 3.5 g of 4-chlorobutyronitrile, 2.3 g of sodium azide and 1.9 g of ammonium chloride in 50 ml of dimethyl-formamide is stirred at 140° C. for 20 hours. The reaction mixture is poured onto ice, basified with 1N sodium hydroxide and extracted twice with ethyl acetate. The aqueous fraction is acidified with acetic acid and extracted with ethylacetate. Evaporation of the ethyl acetate gives 5-(3-chloropropyl)-tetrazole which is used directly in the next step.
Aufarbeitung
- additionThe reaction mixture is poured onto ice
- extractionextracted twice with ethyl acetate
- extractionextracted with ethylacetate
- customEvaporation of the ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-e4e3d5bbcd9a43dfb87623b86425b192
- Quelldatensatz
- uspto-grants-2002_04
- Patentnummer
- US06376512B1
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