反应 #1747859

ord-d521502a280947329879582b45a2df58

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他prepared analogously to Example 13 in U.S
  2. 2
    其他rose from 25 to 43° C
  3. 3
    workup.STIRRINGstirred for 15 min
  4. 4
    过滤filtered through a black band
  5. 5
    过滤filter
  6. 6
    洗涤The residue was washed with 300 ml of methanol
  7. 7
    其他dried 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
    其他purified on silica gel
  10. 10
    其他recrystallized from 83 ml of butylglycol
  11. 11
    其他were obtained

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08029919B2uspto-grants-2011_10