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Hexane → HCID 136156243、化合物

HRID 1032892
ノート
印刷プレビュー

反応式

HRID 1032892 の反応式
[CH:1]1([NH:7][C:8](=[O:24])[C@H:9]([CH:21]([CH3:23])[CH3:22])[NH:10][C:11](OCC2C=CC=CC=2)=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:25]1([C:31]2[CH:38]=[CH:37][CH:36]=[C:33](C=O)[C:32]=2[OH:39])[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.CCCCCC.C(OCC)(=O)C>CO.[C].[Pd]>[CH:1]1([NH:7][C:8](=[O:24])[C@H:9]([CH:21]([CH3:22])[CH3:23])[N:10]=[CH:11][C:33]2[C:32](=[C:31]([C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)[CH:38]=[CH:37][CH:36]=2)[OH:39])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8058HexaneHCID 8857Ethyl AcetateHCID 826228(S)-Benzyl (1-(cyclohexylamino)-3-methyl-1-oxobutan-2-yl)carbamateHCID 107031002-Formyl-6-phenylphenol

生成物 1

HCID 136156243HCID 136156243、化合物収率 76.6%

試薬・触媒・溶媒 2

HCID 178418390
HCID 178418390、化合物
触媒
2 回
HCID 887Methanol溶媒

実験手順

The carbobenzoxy-(S)-valine cyclohexylamide (0.33 g, 1 mmol) was dissolved in methanol (30 ml) and the solution was stirred at room temperature for 3 hours in the presence of 5% palladium-carbon (30 mg) under a hydrogen gas atmosphere. After the reaction was over, the palladium-carbon catalyst was filtered off to obtain a colorless solution. To this solution was added 3-phenylsalicylaldehyde (0.22 g, 1.1 mmol). This solution was stirred at room temperature for 24 hours and concentrated under reduced pressure to obtain yellow solids. These solids were subjected to silica gel column chromatography (eluent; hexane:ethyl acetate=5:1) to obtain 0.29 g (76%) of the desired N-(3-phenylsalicylidene)-(S)-valine cyclohexylamide which was further recrystallized from ether. m.p. 87.0°-89.5° C. [α]26D +158.3° (c 1.02, CHCl3)

後処理

  1. filtrationwas filtered off
  2. customto obtain a colorless solution
  3. concentrationconcentrated under reduced pressure
  4. customto obtain yellow solids

出典と根拠

ORDレコード
ord-1d490d2fca0d4039ad4851e2102700db
出典データセット
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05308820

反応ノート

読み込み中…

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