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Hydroquinone → 4-(Undec-10-EN-1-yloxy)phenol

HRID 863362
ノート
印刷プレビュー

反応式

HRID 863362 の反応式
C1(C)C=CC(S(O[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH:20]=[CH2:21])(=O)=O)=CC=1.[C:23]1([CH:30]=[CH:29][C:27]([OH:28])=[CH:26][CH:25]=1)[OH:24]>C(O)CCC.[Na].[Hg]>[CH2:21]([O:24][C:23]1[CH:30]=[CH:29][C:27]([OH:28])=[CH:26][CH:25]=1)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH:12]=[CH2:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 785HydroquinoneHCID 11141895HCID 11141895、化合物

生成物 1

HCID 183260014-(Undec-10-EN-1-yloxy)phenol収率 47.6%

試薬・触媒・溶媒 2

HCID 9837419Sodium amalgam触媒HCID 2631-Butanol溶媒3 回

反応条件

温度
110 °C

実験手順

2.60 g (8.02 mM) of 10-undecenyl p-toluenesulfonate and 1.79 g (16.2 mM) of hydroquinone were well mixed with 3 ml of butanol under stirring. Into the solution, a solution of 0.419 (9.74 mM) of sodium amalgam dissolved in 6 ml of butanol, followed by 7 hours of heat-refluxing at 110° C. After the reaction, butanol was distilled off, followed by addition of water and extraction with ether. To the ether extract liquid was added anhydrous sodium sulfate for drying, followed by distilling-off of ether and purification by column chromatography (developer solvent: methylene chloride) to obtain 1.00 g (3.82 mM) of p-(10-undecenyl)oxyphenol. Yield: 47.6%.

後処理

  1. distillationwas distilled off
  2. additionfollowed by addition of water and extraction with ether
  3. extractionTo the ether extract liquid
  4. additionwas added anhydrous sodium sulfate
  5. customfor drying
  6. distillationfollowed by distilling-off of ether and purification by column chromatography (developer solvent: methylene chloride)

出典と根拠

ORDレコード
ord-36e3105f15c94d018cd22b164ea99112
出典データセット
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05720898

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート