Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2389생성일: 2026년 10월 23일
Permanganate → (S)-2(isopropylsulfonyl)-amino-3-methyl-butyric acid-N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide
https://huagongshe.com/ko/reaction/2389
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Permanganate | HCID 24401 | — |
| 반응물 | Potassium Permanganate | HCID 516875 | — |
| 반응물 | (S)-2-(isopropylsulfinyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide | HCID 67569267 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | (S)-2(isopropylsulfonyl)-amino-3-methyl-butyric acid-N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide | HCID 67569348 | — |
반응 단계
3.7 g of (S)-2-(isopropylsulfinyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide (Example 3.90) are dissolved in 50 ml of acetone at room temperature. An acetone solution saturated with potassium permanganate is added dropwise to this stirred solution until the reaction mixture retains the violet colour of the permanganate; the reaction mixture is then stirred at room temperature for 45 minutes. The resulting manganese dioxide is removed by filtration over Celite. The filtrate is evaporated to dryness and the resulting residue is dissolved in 500 ml of methyl acetate. This organic phase is washed once with 200 ml of water, dried over sodium sulfate and concentrated. The resulting residue is chromatographed over silica gel with a mixture of one part of methyl acetate and one part of n-hexane. (S)-2-(isopropylsulfonyl)-amino-3-methyl-butyric acid N-[2-(3,4-dimethoxyphenyl)-ethyl]-amide, which can be further purified by recrystallization from methyl acetate/n-hexane, is obtained, melting point 86°-87° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05728875 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-4b5f4cb68ad14383914fad9f4aa70cd0 |
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| 출처 메모 | uspto-grants-1998_03 |
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