Reaktion #5399

ord-5e5c25f893b444bd9bf8ae43f97a4d3f

Reaktionsgleichung

N#Cc1ccc(-c2ccc([C@H]3CC[C@H](O)CC3)cc2)cc1
trans-4-(4'-cyano-4-biphenylyl)cyclohexanol
C1=COCCC1
3,4-dihydro-2H-pyran
C[Si](C)(C)OS(=O)(=O)O[Si](C)(C)C
bistrimethylsilyl sulfate
N#Cc1ccc(-c2ccc([C@H]3CC[C@H](OC4CCCCO4)CC3)cc2)cc1
trans-4-(4'-cyano-4-biphenylyl)cyclohexyl tetrahydropyranyl ether

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed once with sodium carbonate solution and twice with water
  2. 2
    Trocknensubsequently dried over magnesium sulfate
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated
  5. 5
    SonstigeThe crude product was purified by chromatography on silica gel with toluene/ethyl acetate (vol. 9:1)
  6. 6
    SonstigeRecrystallization from ethyl acetate at -20° C.

Vorschrift

A solution of 3.0 g of trans-4-(4'-cyano-4-biphenylyl)cyclohexanol, 1.1 ml of 3,4-dihydro-2H-pyran in 30 ml of dichloromethane was treated at 0° C. with a solution of 0.007 g of bistrimethylsilyl sulfate in 2 ml of dichloromethane. The reaction mixture was stirred at 0° C. for a further 30 minutes and then washed once with sodium carbonate solution and twice with water and subsequently dried over magnesium sulfate, filtered and concentrated. The crude product was purified by chromatography on silica gel with toluene/ethyl acetate (vol. 9:1). Recrystallization from ethyl acetate at -20° C. gave 1.75 g of pure trans-4-(4'-cyano-4-biphenylyl)cyclohexyl tetrahydropyranyl ether.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05244597uspto-grants-1993_09