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Sulfuric Acid → Ethanone, 1-(3-ethyl-4-fluorophenyl)-

HRID 2415258
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HRID 2415258 반응식
OS(O)(=O)=O.[CH2:6]([C:8]1[CH:9]=[C:10]([C:15]#[C:16][Si](C)(C)C)[CH:11]=[CH:12][C:13]=1[F:14])[CH3:7].[O:21]1CCCC1>O.[Hg]=O>[CH2:6]([C:8]1[CH:9]=[C:10]([C:15](=[O:21])[CH3:16])[CH:11]=[CH:12][C:13]=1[F:14])[CH3:7]
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참가 물질

6

반응물 3

HCID 1118Sulfuric Acid2회HCID 8028TetrahydrofuranHCID 22641049(3-Ethyl-4-fluoro-phenylethynyl)-trimethyl-silane

생성물 1

HCID 22641004Ethanone, 1-(3-ethyl-4-fluorophenyl)-

시약·촉매·용매 2

HCID 30856Mercuric oxide촉매HCID 962Water용매

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온도
60 °C

실험 절차

To a stirred solution of H2SO4 (0.25 mL) in H2O (3 mL), HgO (154 mg, 0.712 mmol) was added. Another portion of H2SO4 (0.5 mL) was added so that all of the mercury oxide dissolved. Then the mixture was warmed to 60° C. and (3-ethyl-4-fluoro-phenylethynyl)-trimethyl-silane (1.57 g, 7.12 mmol) was added with tetrahydrofuran (2 mL) during 20 minutes. After the addition, the mixture was stirred for an additional 30 minutes and then cooled and extracted with ether. The extract was passed through a celite pad, washed with saturated brine and dried (Na2SO4). Removal of solvent on a rotary evaporator gave a brown oil, which was chromatographed (25%, dichloromethane/hexanes) to give a yellow oil. 404 mg, 34%.

후처리

  1. dissolutiondissolved
  2. additionAfter the addition
  3. temperaturecooled
  4. extractionextracted with ether
  5. washwashed with saturated brine
  6. dry with materialdried (Na2SO4)
  7. customRemoval of solvent
  8. customon a rotary evaporator
  9. customgave a brown oil, which
  10. customwas chromatographed (25%, dichloromethane/hexanes)
  11. customto give a yellow oil

출처 및 근거

ORD 기록
ord-d58441af837240a58e709886010dab0c
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06818663B2

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