돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35252생성일: 2026년 10월 24일

N-Ethyl cyclohexylamine → HCID 54167384, 화합물

https://huagongshe.com/ko/reaction/35252

반응식

참여 물질

역할이름HCID투입량
반응물N-Ethyl cyclohexylamineHCID 21609—
반응물Isobutyl chloroformateHCID 62365—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물HCID 178482014HCID 178482014—
용매TetrahydrofuranHCID 8028—
생성물HCID 54167384HCID 5416738452%

반응 단계

2-(1-Methyl-1,2,3,4-tetrazol-5-yl)thio-acetic 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 under ice-cooling, and the mixture is further stirred at room temperature for 2 hours. After distilling off the solvent under reduced pressure, the resulting 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 residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-ethyl-N-cyclohexyl-2-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-acetamide (yield: 52%) which is recrystallized from ether-petroleum ether, white prisms, m.p. 69°-71° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766120
출처 데이터셋uspto-grants-1988_08
ORD IDord-b367f873217548f6832be636986c31b9
출처 메모uspto-grants-1988_08