تفاعل #1747859

ord-d521502a280947329879582b45a2df58

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared analogously to Example 13 in U.S
  2. 2
    أخرىrose from 25 to 43° C
  3. 3
    workup.STIRRINGstirred for 15 min
  4. 4
    ترشيحfiltered through a black band
  5. 5
    ترشيحfilter
  6. 6
    غسيلThe residue was washed with 300 ml of methanol
  7. 7
    أخرىdried 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
    أخرىpurified on silica gel
  10. 10
    أخرىrecrystallized from 83 ml of butylglycol
  11. 11
    أخرىwere obtained

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08029919B2uspto-grants-2011_10