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3-Methylcatechol → 5-Methyl-1,4-benzodioxane

HRID 260716
ノート
印刷プレビュー

反応式

HRID 260716 の反応式
[CH3:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:4]([OH:5])[C:3]=1[OH:9].C(=O)([O-])[O-].[K+].[K+].Br[CH2:17][CH2:18]Br>CN(C)C=O>[CH3:1][C:2]1[C:3]2[O:9][CH2:18][CH2:17][O:5][C:4]=2[CH:6]=[CH:7][CH:8]=1
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 3

HCID 3403-MethylcatecholHCID 78391,2-DibromoethaneHCID 11430Potassium Carbonate

生成物 1

HCID 122388275-Methyl-1,4-benzodioxane収率 82%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
125 °C

実験手順

In 300 ml of dry dimethylformamide, was dissolved 30 g of 3-methylcatechol and then 100 g of potassium carbonate was added to the solution. This solution was heated to 120 to 130° C. and 136 g of 1,2-dibromoethane was added dropwise in ten and several portions. After stirring for 30 minutes under the same conditions, the mixture was cooled and solid materials were removed by filtration. To the filtrate, was added diethyl ether, and the mixture was washed successively with a 3% sodium hydroxide aqueous solution, water and saturated saline solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The resulting oily material was purified by silica gel column chromatography to obtain 29.7 g of the titled 5-methyl-1,4-benzodioxane (yield: 82%).

後処理

  1. temperaturethe mixture was cooled
  2. customsolid materials were removed by filtration
  3. additionTo the filtrate, was added diethyl ether
  4. washthe mixture was washed successively with a 3% sodium hydroxide aqueous solution, water and saturated saline solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was removed under reduced pressure
  7. customThe resulting oily material was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-758c32b988024af7807e7840d85e4998
出典データセット
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05530021

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