Reaktion #899

ord-3df2c010cc0541928156900e8959ed27

Reaktionsgleichung

Oc1cccc(C(F)(F)F)c1
m-(trifluoromethyl)phenol
[H-].[Na+]
NaH
CSc1nc(Br)cc(Br)n1
4,6-dibromo-2-(methylthio)pyrimidine
CSc1nc(Br)cc(Oc2cccc(C(F)(F)F)c2)n1
phenoxide
CSc1nc(Br)cc(Oc2cccc(C(F)(F)F)c2)n1
4-bromo-2-methylthio-6-[3-(trifluoromethyl)phenoxy]pyrimidine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONVII-22) (2.0 g, 0.00794 mol) was added
  2. 2
    Sonstigeto react for 5 hours at room temperature

Vorschrift

In THF, a phenoxide was prepared from m-(trifluoromethyl)phenol (1.30 g, 0.00794×1.0 mol) and NaH (0.32 g (ca. 60% in mineral oil), 0.00794×1.0 mol), and 4,6-dibromo-2-(methylthio)pyrimidine (Compound No. VII-22) (2.0 g, 0.00794 mol) was added thereto, and the mixture was then allowed to react for 5 hours at room temperature.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723412uspto-grants-1998_03