Reaktion #1747859

ord-d521502a280947329879582b45a2df58

Reaktionsgleichung

CO
methanol
CC(C)(C)[O-].[K+]
potassium tert-butoxide
CN1c2ccc(C=O)cc2Sc2cc(C=O)ccc21
10-methylphenothiazine-3,7-dicarbaldehyde
CCOP(=O)(OCC)C(c1ccccc1)c1ccccc1
diethyl benzhydrylphosphonate
CN1c2ccc(C=C(c3ccccc3)c3ccccc3)cc2Sc2cc(C=C(c3ccccc3)c3ccccc3)ccc21
3,7-Bis(2,2-diphenylvinyl)-10-methylphenothiazine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeprepared analogously to Example 13 in U.S
  2. 2
    Sonstigerose from 25 to 43° C
  3. 3
    workup.STIRRINGstirred for 15 min
  4. 4
    Filtrationfiltered through a black band
  5. 5
    Filtrationfilter
  6. 6
    WaschenThe residue was washed with 300 ml of methanol
  7. 7
    Sonstigedried at 80° C. under reduced pressure
  8. 8
    workup.DISSOLUTIONThe crude product (4.7 g) was dissolved in 150 ml of methylene chloride
  9. 9
    Sonstigepurified on silica gel
  10. 10
    Sonstigerecrystallized from 83 ml of butylglycol
  11. 11
    Sonstigewere obtained

Vorschrift

3.46 g (30.4 mmol) of potassium tert-butoxide and then 3.60 g (13.4 mmol) of 10-methylphenothiazine-3,7-dicarbaldehyde were added with stirring and at room temperature to a solution of 8.20 g (26.8 mmol) of diethyl benzhydrylphosphonate (prepared analogously to Example 13 in U.S. Pat. No. 5,130,603) in 60 ml of anhydrous dimethyl sulfoxide, in the course of which the temperature rose from 25 to 43° C. After stirring at room temperature for 5 hours, the reaction solution was admixed with 150 ml of methanol, stirred for 15 min and filtered through a black band filter. The residue was washed with 300 ml of methanol and dried at 80° C. under reduced pressure. The crude product (4.7 g) was dissolved in 150 ml of methylene chloride, purified on silica gel and recrystallized from 83 ml of butylglycol. 3.56 g (23% of theory) of greenish microcrystals having a melting point of 233-241° C. were obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08029919B2uspto-grants-2011_10