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

Hydrochloric Acid → 2-Hydroxy-6-(trifluoromethyl)nicotinamide

HRID 658353
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 658353
C[O-].[Na+].[CH2:4]([C:8]([NH2:10])=[O:9])[C:5]([NH2:7])=[O:6].C(O[CH:14]=[CH:15][C:16](=O)[C:17]([F:20])([F:19])[F:18])C.Cl>CO>[O:6]=[C:5]1[C:4]([C:8]([NH2:10])=[O:9])=[CH:14][CH:15]=[C:16]([C:17]([F:20])([F:19])[F:18])[NH:7]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 7911MalonamideHCID 27803954-Ethoxy-1,1,1-trifluoro-3-buten-2-oneHCID 10942334Sodium Methoxide

Produkt 1

HCID 27751142-Hydroxy-6-(trifluoromethyl)nicotinamideAusbeute 83 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887
Methanol
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
45 °C

Versuchsvorschrift

Sodium methoxide (74 g, 1.37 mol) was dissolved in methanol (1,000 mL), and malon diamide (100 g, 0.979 mol) was added to this solution at room temperature. To this mixture, 4-ethoxy-1,1,1-trifluoro-3-buten-2-one (191 g, 1.14 mol) was added dropwise at a temperature between 25 and 30° C., and the resultant mixture was refluxed under heating for 2 hours. After cooling to 45° C., concentrated hydrochloric acid was added to the mixed solution to give a pH of 3 to 4, and 500 mL of methanol was distilled off at normal pressure. To the residue, water (500 mL) was added, and the mixture was stirred for a day at room temperature. The resultant product was precipitated while cooling with ice. Thus obtained crystal was collected by filtration, washed with water, and then dried under reduced pressure, to obtain 167 g of a subject compound (yield: 83%).

Aufarbeitung

  1. temperatureunder heating for 2 hours
  2. distillationwas distilled off at normal pressure
  3. additionTo the residue, water (500 mL) was added
  4. customThe resultant product was precipitated
  5. temperaturewhile cooling with ice
  6. filtrationThus obtained crystal was collected by filtration
  7. washwashed with water
  8. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-34c2b56aba994822b4ca63e566bea97d
Quelldatensatz
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08076487B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion