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Carbon Dioxide → 3-(Trimethylsilyl)butanoic acid

HRID 1655991
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HRID 1655991 반응식
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]
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참가 물질

5

반응물 4

HCID 280Carbon DioxideHCID 3283Diethyl Ether2회HCID 5462224MagnesiumHCID 128458003-Bromopropyltrimethylsilane

생성물 1

HCID 194370223-(Trimethylsilyl)butanoic acid

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-86fcbb84ef1f49f6a1a6d11a5b3f506b
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05252587

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