Water → 4-Bromo-3'-Fluoro-3-Methoxy-1,1'-Biphenyl

HRID 528588

Reaktionsgleichung

Reaktionsgleichung von HRID 528588
[Br:1][C:2]1[CH:7]=[CH:6][C:5](I)=[CH:4][C:3]=1[O:9][CH3:10].[F:11][C:12]1[CH:13]=[C:14](B(O)O)[CH:15]=[CH:16][CH:17]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].O>O1CCOCC1.C(Cl)Cl.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:16]2[CH:15]=[CH:14][CH:13]=[C:12]([F:11])[CH:17]=2)=[CH:4][C:3]=1[O:9][CH3:10]

Komponenten

8

Versuchsvorschrift

A solution of PdCl2(dppf)-CH2Cl2 adduct (0.065 g, 0.080 mmol), 1-bromo-4-iodo-2-methoxybenzene (CombiBlocks, 0.250 g, 0.799 mmol), 3-fluorophenylboronic acid (0.123 g, 0.879 mmol) and potassium phosphate (0.848 g, 3.99 mmol) in dioxane (2.130 ml)/water (1.065 ml) was heated to 90° C. overnight. The reaction was diluted with DCM and separated from the aqueous via phase separator (Radleys Discovery Technologies). After concentration in vacuo, the material was purified via MPLC (12-g Redi Sep Gold), eluting with 0-100% ethyl acetate in heptanes to yield, after concentration, 4-bromo-3′-fluoro-3-methoxy-1,1′-biphenyl as an orange oil, which was used without further purification.

Aufarbeitung

  1. customseparated from the aqueous via phase separator (Radleys Discovery Technologies)
  2. concentrationAfter concentration in vacuo
  3. customthe material was purified via MPLC (12-g Redi Sep Gold)
  4. washeluting with 0-100% ethyl acetate in heptanes
  5. customto yield
  6. concentrationafter concentration, 4-bromo-3′-fluoro-3-methoxy-1,1′-biphenyl as an orange oil, which
  7. customwas used without further purification

Quellen und Nachweise

ORD-Eintrag
ord-a2cb8c1e3c1c4b5f8dc08dffba635e8a
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09346798B2

Verknüpfte Notizen

Wird geladen…