Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35258생성일: 2026년 10월 24일
N-Ethyl cyclohexylamine → N-ethyl-N-cyclohexyl-4-[1-(4-ethylphenyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide
https://huagongshe.com/ko/reaction/35258
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Ethyl cyclohexylamine | HCID 21609 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | HCID 178436515 | HCID 178436515 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-ethyl-N-cyclohexyl-4-[1-(4-ethylphenyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide | HCID 54060908 | 43% |
반응 단계
4-[1-(4-Ethylphenyl)-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 mmol) 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 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 then dried over anhydrous sodium sulfate. Chloroform is distilled off and 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-(4-ethylphenyl)-1,2,3,4-tetrazol-5-yl]thio-butyramide (yield: 43%), colorless liquid, nD19 =1.5533.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04766120 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-9703c3c7166e40c59912450ba1fa4beb |
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| 출처 메모 | uspto-grants-1988_08 |
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