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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35257Erstellt: 24. Oktober 2026

N-Ethyl cyclohexylamine → HCID 21295432, Verbindung

https://huagongshe.com/de/reaction/35257

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Ethyl cyclohexylamineHCID 21609—
EduktIsobutyl chloroformateHCID 62365—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktHCID 178489576HCID 178489576—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 21295432HCID 2129543245%

Reaktionsschritte

4-[1-(2-Methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thio-butyric acid (45 mmole) 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, and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise N-ethyl-cyclohexylamine (54 mmole), and the mixture is further stirred at room temperature for 2 hours. The solvent is distilled off under reduced pressure, and 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 then dried over anhydrous sodium sulfate. After distilling off chloroform, the resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-ethyl-N-cyclohexyl-4-[1-(2-methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thiobutyramide (yield: 45%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04766120
Quelldatensatzuspto-grants-1988_08
ORD IDord-27ca7185f6bc44af8d5416a7ea67b743
Quellennotizuspto-grants-1988_08