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HRID 35251作成日:2026年10月25日

N-Ethyl cyclohexylamine → HCID 54210954、化合物

https://huagongshe.com/reaction/35251

反応式

関与物質

役割名称HCID仕込み量
反応物N-Ethyl cyclohexylamineHCID 21609—
反応物Isobutyl chloroformateHCID 62365—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物HCID 178526181HCID 178526181—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 54210954HCID 5421095443%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04766120
出典データセットuspto-grants-1988_08
ORD IDord-afe70d54050b460998d3b044f17e9b47
出典メモuspto-grants-1988_08