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4-Coumaric acid → 4-Vinylphenol

HRID 327751
ノート
印刷プレビュー

反応式

HRID 327751 の反応式
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7]C(O)=O)=[CH:4][CH:3]=1.C1(C=CC(O)=CC=1)O.N12CCCN=C1CCCCC2>CS(C)=O>[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=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 3224-Coumaric acidHCID 785HydroquinoneHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene

生成物 1

HCID 624534-Vinylphenol

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
135 °C

実験手順

In a 1-liter sulfonating flask equipped with mechanical stirrer, reflux condenser and nitrogen delivery line, 300 ml of dimethyl sulfoxide are added to 150 g (0.91 mol) of 4-hydroxycinnamic acid, 6 g (54 mmol) of hydroquinone and 6 g (39 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene. The mixture is then heated at 135° C. for 31/2 hours. After cooling, the mixture is poured onto ice and extracted three times with 500 ml of diethyl ether, and the organic phase is washed five times with 100 ml of water, dried over magnesium sulfate and concentrated. The resulting oil is recrystallised twice from n-hexane to yield 69.07 g (0.58 mol, 63% of the theoretical yield) of 4-hydroxystyrene in the form of a white powder (m.p. 68° C.).

後処理

  1. customequipped with mechanical stirrer
  2. temperaturereflux condenser
  3. temperatureAfter cooling
  4. additionthe mixture is poured onto ice
  5. extractionextracted three times with 500 ml of diethyl ether
  6. washthe organic phase is washed five times with 100 ml of water
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated
  9. customThe resulting oil is recrystallised twice from n-hexane
  10. customto yield 69.07 g (0.58 mol, 63% of the

出典と根拠

ORDレコード
ord-dee086b3dbe7405ca4cdb115ec555481
出典データセット
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05274060

反応ノート

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