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Water → 4-(3-(Trifluoromethyl)pyridin-2-YL)benzoic acid

HRID 1391426
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1391426
Cl[C:2]1[C:7]([C:8]([F:11])([F:10])[F:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[C:12](=[O:15])([O-])[O-:13].[K+].[K+].O.[C:19](#N)[CH3:20]>[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[F:9][C:8]([F:11])([F:10])[C:7]1[C:2]([C:20]2[CH:19]=[CH:7][C:6]([C:12]([OH:13])=[O:15])=[CH:5][CH:4]=2)=[N:3][CH:4]=[CH:5][CH:6]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 6342AcetonitrileHCID 11430Potassium CarbonateHCID 5898332-Chloro-3-(trifluoromethyl)pyridine

Produkt 1

HCID 534262354-(3-(Trifluoromethyl)pyridin-2-YL)benzoic acidAusbeute 81 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 11979704
Tetrakis(triphenylphosphine)palladium
Katalysator

Reaktionsbedingungen

Temperatur
160 °C

Versuchsvorschrift

4-Bis(hydroxyl)boron-1-methylbenzoate (2.8 mmol) was dissolved in acetonitrile (2 ml) and added to a 5 ml microwave vessel. To the solution was 3.5 mmol of 2-chloro-3-trifluoromethylpyridine (633 mg), 34 mg of tetrakis(triphenylphosphine)-palladium(0). After stirring until dissolution, 8.4 mmol of potassium carbonate (1.16 g) was added, followed by 1 ml of water. The mixture was then heated at 160° C. for 300 seconds. After reaction completion, the solvents were evaporated under vacuum. The residue was dissolved in 2N KOH and THF and heated for 10 min. After hydrolysis, the THF was evaporated and the basic layer was washed with EtOAC. The aqueous layer was then acidified and extracted 3 times with EtOAc. The organic layers were combined and washed with water and brine. After drying, filtration and evaporation, the residue was prufied by HPLC to give of the target compound as a white solid (602 mg; 81%).

Aufarbeitung

  1. additionadded to a 5 ml microwave vessel
  2. additionwas added
  3. customAfter reaction completion
  4. customthe solvents were evaporated under vacuum
  5. dissolutionThe residue was dissolved in 2N KOH
  6. temperatureTHF and heated for 10 min
  7. customAfter hydrolysis
  8. customthe THF was evaporated
  9. washthe basic layer was washed with EtOAC
  10. extractionextracted 3 times with EtOAc
  11. washwashed with water and brine
  12. customAfter drying
  13. filtrationfiltration and evaporation

Quellen und Nachweise

ORD-Eintrag
ord-bf01f8c01679416abdc35f0a9cbe5046
Quelldatensatz
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07338950B2

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