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

Hydrochloric Acid → HCID 86047684, Verbindung

HRID 554251
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 554251
[F:1][C:2]([F:14])([F:13])[S:3]([C:6]1[CH:7]=[C:8](N)[CH:9]=[CH:10][CH:11]=1)(=[O:5])=[O:4].[ClH:15].N([O-])=O.[Na+].[S:20](=[O:22])=[O:21]>>[F:1][C:2]([F:14])([F:13])[S:3]([C:6]1[CH:7]=[C:8]([S:20]([Cl:15])(=[O:22])=[O:21])[CH:9]=[CH:10][CH:11]=1)(=[O:5])=[O:4]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 313Hydrochloric AcidHCID 1119Sulfur DioxideHCID 27359433-Aminophenyl trifluoromethyl sulfoneHCID 23668193Sodium Nitrite

Produkt 1

HCID 86047684HCID 86047684, VerbindungAusbeute 79 %

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

Under ice-cooling, thionyl chloride (4 mL) was added dropwise to water (24 mL) over 30 min. The mixture was stirred at room temperature for 12 hr to give a sulfur dioxide-containing solution. Under ice-cooling, {3-[(trifluoromethyl)sulfonyl]phenyl}amine (1.0 g) was added to concentrated hydrochloric acid (6 mL) and the mixture was stirred. An aqueous solution (2 mL) of sodium nitrite (0.34 g) was added dropwise while maintaining the inside temperature at not higher than 5° C. and the mixture was further stirred for 15 min. The mixture was gradually added at 5° C. to a mixture of the above-mentioned sulfur dioxide-containing solution added with cuprous chloride (10 mg). Under ice-cooling, the mixture was further stirred for 30 min, and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→7:3) to give the title compound as a pale-yellow oil (yield 1.08 g, 79%).

Aufarbeitung

  1. additioncontaining solution
  2. temperatureUnder ice-cooling
  3. stirringthe mixture was further stirred for 15 min
  4. additioncontaining solution
  5. temperatureUnder ice-cooling
  6. stirringthe mixture was further stirred for 30 min
  7. extractionextracted with ethyl acetate
  8. dry with materialThe extract was dried over anhydrous magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→7:3)

Quellen und Nachweise

ORD-Eintrag
ord-7b4bf8d6595340279ecc123809f300af
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08048909B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion