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Sodium Carbonate → 2'-(2,4,6-Trimethoxybenzylthio)biphenyl-3-ol

HRID 1158198
ノート
印刷プレビュー

反応式

HRID 1158198 の反応式
[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[C:16]([O:22][CH3:23])[C:4]=1[CH2:5][S:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1B(O)O.I[C:25]1[CH:26]=[C:27]([OH:31])[CH:28]=[CH:29][CH:30]=1.C([O-])([O-])=O.[Na+].[Na+]>[Pd].C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[C:16]([O:22][CH3:23])[C:4]=1[CH2:5][S:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([OH:31])[CH:26]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10340Sodium CarbonateHCID 122723-IodophenolHCID 686436172-(2,4,6-Trimethoxybenzylthio)phenylboronic acid

生成物 1

HCID 668706052'-(2,4,6-Trimethoxybenzylthio)biphenyl-3-ol収率 79%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 1140Toluene
溶媒

実験手順

To a mixture of 1.05 g 2-(2,4,6-trimethoxybenzylthio)phenylboronic acid (3.14 mmol), 1.07 g 3-iodophenol (4.9 mmol) and 0.195 g Pd catalyst was added 40 ml toluene followed by 15 ml 2M Na2CO3. The mixture was refluxed under nitrogen overnight. The mixture was extracted with ethyl acetate. The organic was washed with water, brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica flash chromatography (hexane:ethyl acetate 80:20) to afford 0.948 g product (2.48 mmol, 79% yield).

後処理

  1. temperatureThe mixture was refluxed under nitrogen overnight
  2. extractionThe mixture was extracted with ethyl acetate
  3. washThe organic was washed with water, brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customThe residue was purified by silica flash chromatography (hexane:ethyl acetate 80:20)

出典と根拠

ORDレコード
ord-34f6d060a05d4add8cd5024d6db21943
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07807713B2

反応ノート

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