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Carbon Dioxide → 3-(Trimethylsilyl)butanoic acid

HRID 1655991
ノート
印刷プレビュー

反応式

HRID 1655991 の反応式
BrC[CH2:3][CH2:4][Si:5]([CH3:8])([CH3:7])[CH3:6].[Mg].[C:10](=[O:12])=[O:11].[CH3:13]COCC>>[CH3:6][Si:5]([CH3:8])([CH3:7])[CH:4]([CH3:13])[CH2:3][C:10]([OH:12])=[O:11]
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 4

HCID 280Carbon DioxideHCID 3283Diethyl Ether2 回HCID 5462224MagnesiumHCID 128458003-Bromopropyltrimethylsilane

生成物 1

HCID 194370223-(Trimethylsilyl)butanoic acid

実験手順

A solution containing 3 g (15.4 mmol) of (3-bromopropyl)trimethylsilane in 3 ml of dry ether was added to 0.375 g (15.4 mmol) of magnesium turnings in ether (40 ml final volume of solution). After 1 hour of reflux gazeous carbondioxide was bubbled through the reaction mixture (3 g, 77 mmol of dry ice). After 2 hours of stirring at room temperature the reaction mixture was partitioned between aqueous ammonium chloride and ether. The organic phase was separated, the aqueous phase was further acidified with hydrochloric acid 1N and extracted with ether. Ethereal phases were pooled and the solvent was removed under reduced pressure. Separation of the expected 4-trimethylsilylbutanoic acid from dimer of starting (3-bromopropyl)trimethylsilane was finally performed by acid base extraction. 0.62 g of 3-(trimethylsilyl)-butanoic acid was isolated as a colorless liquid.

後処理

  1. customwas partitioned between aqueous ammonium chloride and ether
  2. customThe organic phase was separated
  3. extractionextracted with ether
  4. customthe solvent was removed under reduced pressure
  5. customSeparation of the expected 4-trimethylsilylbutanoic acid from dimer of starting (3-bromopropyl)trimethylsilane
  6. extractionwas finally performed by acid base extraction

出典と根拠

ORDレコード
ord-86fcbb84ef1f49f6a1a6d11a5b3f506b
出典データセット
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05252587

反応ノート

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