1-Chloro-4-(trifluoromethyl)benzene → 4-Methoxy-4'-trifluoromethyl-biphenyl

HRID 607914

Reaktionsgleichung

Reaktionsgleichung von HRID 607914
COc1ccc(B(O)O)cc1.FC(F)(F)c1ccc(Cl)cc1>C1=C\CC/C=C\CC/1.C1=C\CC/C=C\CC/1.C1COCCO1.COc1ccc(OC)c(P(c2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)c1-c1c(C(C)C)cc(C(C)C)cc1C(C)C.O.O=P([O-])([O-])[O-].[K+].[K+].[K+].[Ni]>COc1ccc(-c2ccc(C(F)(F)F)cc2)cc1

Komponenten

8

Edukt 2

HCID 73941-Chloro-4-(trifluoromethyl)benzeneHCID 201262(4-Methoxyphenyl)boronic acid

Produkt 1

HCID 112074784-Methoxy-4'-trifluoromethyl-biphenylAusbeute 17 %

Reagenzien, Katalysatoren, Lösungsmittel 5

HCID 962WaterReagenzHCID 62657Potassium Phosphate, TribasicReagenzHCID 6433264Bis(1,5-cyclooctadiene)nickelKatalysatorHCID 44597232Bis(3,5-bis(trifluoromethyl)phenyl)(3,6-dimethoxy-2',4',6'-tri(propan-2-yl)(1,1'-biphenyl)-2-yl)phosphaneKatalysatorHCID 312751,4-DioxaneLösungsmittel4×

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

pre-ligate Ni(cod)2 and phosphine ligand in dioxane for 15 minutes in a separate plate

Aufarbeitung

  1. additionDilute with acetonitrile
  2. aliquotKeine Vorschrift aufgezeichnet
  3. customDiluent solution was made in 1 L batches with 950 mL acetonitrile, 25 mL water, 25 mL glacial acetic acid, and 53 mg 4,4’-di-tert-butylbiphenyl as an external standard (0.2 equiv standard per reaction). Aliquot taken from each well (47 ul) is added into 753 ul of diluent solution

Quellen und Nachweise

ORD-Eintrag
ord-0a99f730b8204d8289f51a940398a1f9
Quelldatensatz
Ni-catalyzed Suzuki Miyaura cross-coupling
Originallink
Quelle ansehen

Verknüpfte Notizen

Wird geladen…