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HRID 35251Erstellt: 23. Oktober 2026

N-Ethyl cyclohexylamine → HCID 54210954, Verbindung

https://huagongshe.com/de/reaction/35251

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Ethyl cyclohexylamineHCID 21609—
EduktIsobutyl chloroformateHCID 62365—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktHCID 178526181HCID 178526181—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 54210954HCID 5421095443%

Reaktionsschritte

4-(1-Phenyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (45 mmol) is dissolved in tetrahydrofuran (50 ml) and thereto is added DBU (50 mmole). To the mixture is added dropwise with stirring isobutyl chloroformate (50 mmole) under ice-cooling. The mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise N-ethylcyclohexylamine (54 mmole) and the mixture is further stirred at room temperature for 2 hours. After distilling off the solvent under reduced pressure, the residue is extracted with chloroform. The chloroform layer is washed with 5% aqueous hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution and an aqueous saturated sodium chloride solution and dried over anhydrous sodium sulfate. Chloroform is distilled off and the resulting residue is subjected to column chromatogrophy (Wakogel C-200, eluting solvent, chloroform) to isolate N-ethyl-N-cyclohexyl-4-(1-phenyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (yield: 43%), colorless liquid, nD18 =1.5590.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04766120
Quelldatensatzuspto-grants-1988_08
ORD IDord-afe70d54050b460998d3b044f17e9b47
Quellennotizuspto-grants-1988_08