Réaction #93673

ord-1a164770ec224eafbc80dfc3dde7daea

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureby heating
  2. 2
    Autreat 120° C.
  3. 3
    Autrefor one hour
  4. 4
    Températurecooling
  5. 5
    workup.ADDITIONadding, at a stroke
  6. 6
    Autreat 50° C.
  7. 7
    workup.DISTILLATIONdistilling off so that the temperature of the system
  8. 8
    Autremight become 200° C.
  9. 9
    Températurecooling
  10. 10
    workup.ADDITIONadding water (200 ml) and toluene (50 ml)
  11. 11
    Lavagewater-washing the organic layer till the washing liquid
  12. 12
    workup.DISTILLATIONdistilling off the solvent
  13. 13
    workup.DISTILLATIONdistilling under reduced pressure
  14. 14
    Autreto collect a fraction
  15. 15
    Autrerecrystallizing it from ethyl alcohol (20 ml) and ethyl acetate (5 ml)

Mode opératoire

4-Octyloxy-4'-((S)-3-methyl-pentanoyl)biphenyl (24.6 g, 0.065 mol) obtained in Example 23 described later, 80% hydrazine hydrate (50 ml) and diethylene glycol (85 ml) were placed in a 500 ml three-neck flask, followed by heating with stirring, keeping the mixture at 120° C. for one hour, then cooling, adding, at a stroke, a solution of potassium hydroxide (8.8 g, 0.157 mol) in water (5 ml) while keeping the temperature at 50° C., distilling off so that the temperature of the system might become 200° C., reacting at 200° C. for 4 hours, then cooling, adding water (200 ml) and toluene (50 ml), transferring the contents into a separating funnel, water-washing the organic layer till the washing liquid became neutral, distilling off the solvent, distilling under reduced pressure to collect a fraction having a boiling point of 210°~213° C./3 mmHg, and recrystallizing it from ethyl alcohol (20 ml) and ethyl acetate (5 ml) to obtain 4-octyloxy-4'-((S)-3-methyl-pentyl)biphenyl (IIIb1) (13.5 g) which was a smectic liquid crystal exhibiting SC* phase and SH* phase, and whose phase transition points were as follows as shown in Table 2, column of Example 24:

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04614609uspto-grants-1986_09