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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35254생성일: 2026년 10월 24일

Methyl chloroformate → N-(4-methoxycyclohexyl)-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide

https://huagongshe.com/ko/reaction/35254

반응식

참여 물질

역할이름HCID투입량
반응물Methyl chloroformateHCID 6586—
반응물4-MethylmorpholineHCID 7972—
반응물2-Methoxycyclohexan-1-amineHCID 22250879—
반응물HCID 178482013HCID 178482013—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-(4-methoxycyclohexyl)-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramideHCID 5379085143%

반응 단계

To methylene chloride (50 ml) are added 4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (45 mmole) and N-methylmorpholine (50 mmole). To the mixture is added dropwise with stirring methyl chloroformate (50 mmole) with keeping the inner temperature at 10°-20° C. by ice-cooling, and thereafter, the mixture is stirred at room temperature for 30 minutes. To the mixture is added 2-methoxycyclohexylamine (54 mmole), and the mixture is stirred at the same temperature for 4 hours. After the reaction, water is added to the reaction mixture. The organic layer is separated and washed with dilute aqueous sodium hydroxide solution, diluted hydrochloric acid and water in order, and dried over sodium sulfate. Inorganic materials are filtered off, and the mother liquor is concentrated. The resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-(4-methoxycyclohexyl)-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (yield: 43%), colorless liquid, nD11 =1.5263.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766120
출처 데이터셋uspto-grants-1988_08
ORD IDord-f211f03e53b04a2a9cb7041bab37de39
출처 메모uspto-grants-1988_08