StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

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

HRID 2415258
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2415258
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]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 1118Sulfuric Acid2×HCID 8028TetrahydrofuranHCID 22641049(3-Ethyl-4-fluoro-phenylethynyl)-trimethyl-silane

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 30856Mercuric oxideKatalysator
HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

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%.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-d58441af837240a58e709886010dab0c
Quelldatensatz
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06818663B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion