Reaktion #344033

ord-1f4412de9f8c46e8b26286e15b0fee82

Reaktionsgleichung

C#CC1(C)CCc2c(C)c(O)c(C)c(C)c2O1
rac-3,4-dihydro-2-ethynyl-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol
Fc1ccc(Br)cc1F
1-bromo-3,4-difluorobenzene
Cc1c(C)c2c(c(C)c1O)CCC(C)(C#Cc1ccc(F)c(F)c1)O2
rac-2-[(3,4-Difluorophenyl)ethynyl]-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto 42 hours
  2. 2
    Sonstigegave
  3. 3
    Sonstigeafter chromatographic isolation (40 fold amount of silica gel using methylene chloride) and crystallization from petroleum ether colorless crystals of the title compound with m.p. 109°-112°

Vorschrift

Reaction of rac-3,4-dihydro-2-ethynyl-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol with 1-bromo-3,4-difluorobenzene under the conditions described in Example 26 and extending the reaction time to 42 hours gave after chromatographic isolation (40 fold amount of silica gel using methylene chloride) and crystallization from petroleum ether colorless crystals of the title compound with m.p. 109°-112°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05260294uspto-grants-1993_11