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

HRID 1905320
ノート
印刷プレビュー

反応式

HRID 1905320 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

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

実験手順

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.

後処理

  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)
  • 出典と根拠

    ORDレコード
    ord-0195243b3e794b95aaf51e9fde99fcb2
    出典データセット
    uspto-grants-1989_06
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04841067

    反応ノート

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