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Dimethyl Sulfoxide → 1-Ethenyl-4-(2-methylpropyl)benzene

HRID 1065535
ノート
印刷プレビュー

反応式

HRID 1065535 の反応式
[CH2:1]([C:5]1[CH:10]=[CH:9][C:8]([CH:11](O)[CH3:12])=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3].CS(C)=O>O.[N+](C1C=CC=C([N+]([O-])=O)C=1)([O-])=O>[CH2:1]([C:5]1[CH:6]=[CH:7][C:8]([CH:11]=[CH2:12])=[CH:9][CH:10]=1)[CH:2]([CH3:4])[CH3:3]
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 679Dimethyl SulfoxideHCID 1816541-(4-Isobutylphenyl)ethanol

生成物 1

HCID 5761461-Ethenyl-4-(2-methylpropyl)benzene収率 77.9%

試薬・触媒・溶媒 2

HCID 74521,3-Dinitrobenzene触媒HCID 962Water溶媒

反応条件

温度
160 °C

実験手順

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

To 6 g of α-(4-isobutylphenyl)ethyl alcohol were added 12 g of dimethyl sulfoxide and 0.1 g of m-dinitrobenzene as a polymerization inhibitor. The mixture was stirred at 160° C. for 8 hours. The resultant reaction liquor was cooled, diluted with water and then subjected to extraction with benzene. After the resulting organic layer was dried with magnesium sulfate, the solvent was distilled off. The residue thus obtained was distilled to give 4.2 g of 4-isobutylstyrene having the following physical properties.

後処理

  1. customThe resultant reaction liquor
  2. temperaturewas cooled
  3. extractionsubjected to extraction with benzene
  4. dry with materialAfter the resulting organic layer was dried with magnesium sulfate
  5. distillationthe solvent was distilled off
  6. customThe residue thus obtained
  7. distillationwas distilled

出典と根拠

ORDレコード
ord-4f7cd24f87a6423989f723a73b4ad459
出典データセット
uspto-grants-1982_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04329507

反応ノート

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