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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → Methylphenyldivinylsilane

HRID 40550
ノート
印刷プレビュー

反応式

HRID 40550 の反応式
C([Mg]Cl)=C.CO[CH:7]([Si:10]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)([CH:13]=[CH2:14])[CH:11]=[CH2:12])OC.O>C1COCC1>[CH3:7][Si:10]([C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)([CH:11]=[CH2:12])[CH:13]=[CH2:14]
参加物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 962WaterHCID 66926031DimethoxymethylphenyldivinylsilaneHCID 178461836HCID 178461836、化合物

生成物 1

HCID 594382Methylphenyldivinylsilane

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

158 ml of a solution of vinylmagnesium chloride in THF is added dropwise using a dropping funnel in 1 h at room temperature under nitrogen to 13.1 ml of a solution of dimethoxymethylphenyldivinylsilane in 36 ml of anhydrous THF. The temperature is controlled with a water bath. After addition, the mixture is stirred at room temperature for 16 h and then refluxed for 2 h. 40 ml of H2O is then added and the mixture is stirred for 30 min. The white precipitate that forms is filtered and is then rinsed with ethyl acetate. The filtrate is extracted with ethyl acetate twice. The organic phases are combined, washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated under vacuum. 12.56 g of methyl-phenyl-divinyl-silane is obtained in the form of a clear yellow oil, which is then used without further purification.

後処理

  1. customin 1 h
  2. customat room temperature
  3. customThe temperature is controlled with a water bath
  4. additionAfter addition
  5. temperaturerefluxed for 2 h
  6. stirringthe mixture is stirred for 30 min
  7. filtrationThe white precipitate that forms is filtered
  8. washis then rinsed with ethyl acetate
  9. extractionThe filtrate is extracted with ethyl acetate twice
  10. washwashed with a saturated aqueous solution of sodium chloride
  11. dry with materialdried over magnesium sulfate
  12. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-55773ef170c04647a895f9feb8385b27
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08530473B2

反応ノート

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