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Methanol → (2RS, 3S)-3-carbobenzoxyamino-2-hydroxy-5-methylhexyl methyl ether

HRID 1905320
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HRID 1905320 반응식
[C:1]([NH:11][C@@H:12]([CH2:16][CH:17]([CH3:19])[CH3:18])[CH:13]1[O:15][CH2:14]1)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].[CH3:20][OH:21]>>[CH3:20][O:21][CH2:14][CH:13]([OH:15])[C@@H:12]([NH:11][C:1]([O:3][CH2:4][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1)=[O:2])[CH2:16][CH:17]([CH3:18])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 887MethanolHCID 13909433(3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexane

생성물 1

HCID 13909435(2RS, 3S)-3-carbobenzoxyamino-2-hydroxy-5-methylhexyl methyl ether

실험 절차

To a solution of 176 mg of (3S)-3-carbobenzoxyamino-5-methyl-1,2-epoxyhexane in 10 ml of methanol was added 2 g of dry neutral alumina, and the mixture was heated under reflux for 16 hours. After filtration of the alumina, the filtrate was evaporated under reduced pressure. The residue was purified by preparative silica gel thin layer chromatography (developing solvent: lower layer of chloroform/methanol/water=8/3/1 by volume) to obtain 96 mg of (2RS, 3S)-3-carbobenzoxyamino-2-hydroxy-5-methylhexyl methyl ether as a colorless viscous oil.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 16 hours
  3. filtrationAfter filtration of the alumina
  • customthe filtrate was evaporated under reduced pressure
  • customThe residue was purified by preparative silica gel thin layer chromatography (developing solvent: lower layer of chloroform/methanol/water=8/3/1 by volume)
  • 출처 및 근거

    ORD 기록
    ord-0195243b3e794b95aaf51e9fde99fcb2
    출처 데이터셋
    uspto-grants-1989_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04841067

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