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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978029Generated: October 25, 2026

N-Ethyl cyclohexylamine → HCID 21295432, compound

https://huagongshe.com/reaction/978029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Ethyl cyclohexylamineHCID 21609—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178489576HCID 178489576—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21295432HCID 2129543245%

Reaction Steps

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:chlororform=4:1, V/V) to isolate N-ethyl-N-cyclohexyl-4-[1-(2-methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide (yield: 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663323
Source datasetuspto-grants-1987_05
ORD IDord-d0c1a78f34f34ebda184f304400986e1
Source noteuspto-grants-1987_05