Reaktion #4222

ord-65ac7b4e119c45f7be18d6fb28021e3d

Reaktionsgleichung

CC(C)(C)C1(C=Cc2ccc(Cl)cc2)CO1
2-(4-chlorophenyl-ethenyl)-2-tert.-butyl-oxirane
c1nc[nH]n1
1,2,4-triazole
CCO
ethanol
CC(C)(C)C(O)(C=Cc1ccc(Cl)cc1)Cn1ccnc1
1-(4-chlorophenyl)-4,4-dimethyl-3-(imidazol-1-yl-methyl)-1-penten-3-ol
Ausbeute 77.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe reaction mixture was then concentrated
  2. 2
    FiltrationThe solid was then filtered off
  3. 3
    Sonstigerecrystallised from acetonitrile

Vorschrift

A solution of 17.75 g (0.075 mole) of 2-(4-chlorophenyl-ethenyl)-2-tert.-butyl-oxirane and 6.9 g (0.1 mole) of 1,2,4-triazole in 30 ml of ethanol was heated in a bomb tube at 150° C. for 20 hours. The reaction mixture was then concentrated and the crystalline residue was stirred with ether. The solid was then filtered off and recrystallised from acetonitrile. 17.7 g (77% of theory) of 1-(4-chlorophenyl)-4,4-dimethyl-3-(imidazol-1-yl-methyl)-1-penten-3-ol of melting point 139°-41° C. were obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723984uspto-grants-1988_02