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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35257생성일: 2026년 10월 24일

N-Ethyl cyclohexylamine → HCID 21295432, 화합물

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

반응식

참여 물질

역할이름HCID투입량
반응물N-Ethyl cyclohexylamineHCID 21609—
반응물Isobutyl chloroformateHCID 62365—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물HCID 178489576HCID 178489576—
용매TetrahydrofuranHCID 8028—
생성물HCID 21295432HCID 2129543245%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766120
출처 데이터셋uspto-grants-1988_08
ORD IDord-27ca7185f6bc44af8d5416a7ea67b743
출처 메모uspto-grants-1988_08