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

Formamide → 2-Fluoro-4-(thiazol-4-yl)phenol

HRID 1597610
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1597610
P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=S.C(N)=O.Br[CH2:19][C:20]([C:22]1[CH:27]=[CH:26][C:25]([OH:28])=[C:24]([F:29])[CH:23]=1)=O.[CH:30]([NH2:32])=[S:31].[OH-].[Na+]>O1CCOCC1>[F:29][C:24]1[CH:23]=[C:22]([C:20]2[N:32]=[CH:30][S:31][CH:19]=2)[CH:27]=[CH:26][C:25]=1[OH:28]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 713FormamideHCID 14798Sodium HydroxideHCID 14817Phosphorus sulfide (P2S5)HCID 3005587MethanethioamideHCID 179235302-Bromo-1-(3-fluoro-4-hydroxyphenyl)ethan-1-one

Produkt 1

HCID 223169222-Fluoro-4-(thiazol-4-yl)phenolAusbeute 83 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel2×

Versuchsvorschrift

To a stirred solution of phosphorus pentasulfide (8.6 g, 19.3 mmol) in dioxane (53 ml) was added formamide (5.2 g, 115.5 mmol), and the mixture was heated at reflux temperature for 2 hours. The mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2-bromo-1-(3-fluoro-4-hydroxyphenyl)-1-ethanone (3.02 g, 12.98 mmol) in dioxane (50 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The mixture was cooled down to room temperature, and made basic by addition of 0.5M NaOH aqueous solution. The whole was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:3) to give title compound (2.11 g, 83% yield).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureat reflux temperature for 2 hours
  3. customthe solution was decanted away from solids
  4. temperaturethe mixture was heated
  5. temperatureat reflux temperature for 6 hours
  6. temperatureThe mixture was cooled down to room temperature
  7. extractionThe whole was extracted with ethyl acetate
  8. washThe organic layer was washed with brine
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated in vacuo
  11. customThe residue was purified by flash chromatography
  12. washeluting with ethyl acetate-hexane (1:3)

Quellen und Nachweise

ORD-Eintrag
ord-11d69ac94c6f47ba9bbc46f9b9e387e2
Quelldatensatz
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06294558B1

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion