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Phenylboronic Acid → 5-(Trifluoromethyl)biphenyl-2-carboxylic acid

HRID 560212
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 560212
Br[C:2]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[C:15]1(B(O)O)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC)=CC=CC=2OC)CCCCC1>O1CCOCC1.C(=O)([O-])[O-].[Na+].[Na+].C(OCC)(=O)C.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[F:12][C:11]([F:14])([F:13])[C:9]1[CH:10]=[C:2]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:3]([C:4]([OH:6])=[O:5])=[CH:7][CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 3

HCID 66827Phenylboronic AcidHCID 676052-Bromo-4-(trifluoromethyl)benzoic acidHCID 112698722-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl

Produkt 1

HCID 463151975-(Trifluoromethyl)biphenyl-2-carboxylic acidAusbeute 64 %

Reagenzien, Katalysatoren, Lösungsmittel 5

HCID 167845palladium(II) acetate
Katalysator
HCID 962WaterLösungsmittel
HCID 8857Ethyl AcetateLösungsmittel
HCID 10340Sodium CarbonateLösungsmittel2×
HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

2-Bromo-4-trifluoromethyl-benzoic acid (100 mg, 0.372 mmol) and phenylboronic acid (70 mg, 0.574 mmol) were dissolved in 6 mL dioxane and 3 mL 1N sodium carbonate solution. The mixture was evacuated and back-filled with argon several times to remove oxygen. 2-Dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (S-Phos, 31 mg, 0.075 mmol) and palladium acetate (8 mg, 0.036 mmol) were added and the reaction mixture was refluxed overnight. The mixture was diluted with ethyl acetate, water and 2N sodium carbonate solution. The mixture was extracted three times with 2N sodium carbonate solution and the aqueous layers washed with ethyl acetate. The combined organic layers were discarded. The combined aqueous layers were acidified with 2N HCl and extracted twice with dichloromethane. The organic layers were washed with brine, combined, dried over sodium sulfate, filtered and concentrated down. Purification of the residue by flash chromatography on gel with dichloromethane/methanol/acetic acid (100:0:0→90:10:0.5) yielded the title compound as a white solid (63 mg, 64%).

Aufarbeitung

  1. customThe mixture was evacuated
  2. additionback-filled with argon several times
  3. customto remove oxygen
  4. temperaturethe reaction mixture was refluxed overnight
  5. extractionThe mixture was extracted three times with 2N sodium carbonate solution
  6. washthe aqueous layers washed with ethyl acetate
  7. extractionextracted twice with dichloromethane
  8. washThe organic layers were washed with brine
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated down
  12. customPurification of the residue by flash chromatography on gel with dichloromethane/methanol/acetic acid (100:0:0→90:10:0.5)

Quellen und Nachweise

ORD-Eintrag
ord-e7105b84f02b48c29515306a11f84846
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08063098B2

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