Sulfuric Acid → 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-

HRID 727474

反応式

HRID 727474 の反応式
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[C:4]([CH3:9])[C:3]=1[OH:10].S([O-])(O[O-])(=O)=[O:12].[K+].[K+].S(=O)(=O)(O)O>C(O)(=O)C.O>[CH3:8][C:7]1[C:6](=[O:12])[CH:5]=[C:4]([CH3:9])[C:3](=[O:10])[C:2]=1[CH3:1]

参加物

6

反応物 3

HCID 1118Sulfuric AcidHCID 170162,3,6-TrimethylphenolHCID 10313463Potassium peroxymonosulphate

生成物 1

HCID 702912,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-収率 74%

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒2 回HCID 962Water溶媒

実験手順

A solution of 13.6 g (100 mmol) of 2,3,6-trimethylphenol in 40 ml of acetic acid and a solution of 73.7 g (240 mmol) of 50% by weight potassium peroxomonosulfate in 320 ml of water were simultaneously added dropwise to a stirred solution of 0.68 g (2.0 mmol) of iron 5,14-dihydrodibenzo[b,i][5,9,14,18]tetraaza[14]annulene and 0.5 ml of concentrated sulfuric acid in 50 ml of acetic acid at room temperature with cooling. The reaction mixture was then subjected to steam distillation. The distillate was extracted by shaking with methylene chloride. The organic phase was shaken with aqueous sodium bicarbonate solution and then with water, separated from the aqueous phase, dried over magnesium sulfate, filtered and concentrated to a yellow oil, which slowly solidifed. 11.1 g (74%) of 2,3,5-trimethyl-p-benzoquinone were obtained in the form of yellow oily crystals.

後処理

  1. temperaturewith cooling
  2. distillationThe reaction mixture was then subjected to steam distillation
  3. extractionThe distillate was extracted
  4. stirringThe organic phase was shaken with aqueous sodium bicarbonate solution
  5. customwith water, separated from the aqueous phase
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated to a yellow oil, which

出典と根拠

ORDレコード
ord-9da68dad0b324541961fdd825f05dd61
出典データセット
uspto-grants-1998_01
特許番号
US05712416

関連ノート

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