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Potassium Hydroxide → 4-Chloro-2-ethynyl-1-methoxybenzene

HRID 1616598
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HRID 1616598 반응식
[OH-].[K+].[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([O:16][CH3:17])=[C:8]([C:10]#[C:11][Si](C)(C)C)[CH:9]=1>O.CO>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([O:16][CH3:17])=[C:8]([C:10]#[CH:11])[CH:9]=1
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참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 68489883[2-(5-Chloro-2-methoxyphenyl)ethynyl]trimethylsilane

생성물 1

HCID 232607034-Chloro-2-ethynyl-1-methoxybenzene수율 135.9%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

Add a solution of potassium hydroxide (3.28 g, 58.5 mmol) in water (30 mL) dropwise over 25 minutes to a stirred solution of (5-chloro-2-methoxy-phenylethynyl)-trimethylsilane (13.7 g, 57.4 mmol) in methanol (275 mL) and stir at room temperature for 2 hours. Concentrate, add brine to residue, and extract with EtOAc (×2). Dry organic layer over MgSO4 and concentrate to get 13 g of a black oil. Adsorb on SiO2 and purify the residue by flash chromatography on silica gel eluting with 0-5% EtOAc/hexanes to afford the title compound (8.98 g, 94%).

후처리

  1. concentrationConcentrate
  2. additionadd brine to residue
  3. extractionextract with EtOAc (×2)
  4. concentrationDry organic layer over MgSO4 and concentrate

출처 및 근거

ORD 기록
ord-cc99cd129ade4e35966ccc18acbd5af2
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765796B2

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