反应 #1747863

ord-616823c9315c48d49335187d1b6f8b18

反应方程式

CC(C)(C)[O-].[K+]
potassium tert-butoxide
O=Cc1ccc2c(c1)Sc1ccccc1N2c1ccccc1
10-phenylphenothiazine-3-carbaldehyde
CCOP(=O)(Cc1ccc(-c2ccc(CP(=O)(OCC)OCC)cc2)cc1)OCC
diethyl[4′-(diethoxyphosphorylmethyl)biphenyl-4-ylmethyl]phosphonate
C(=Cc1ccc2c(c1)Sc1ccccc1N2c1ccccc1)c1ccc(-c2ccc(C=Cc3ccc4c(c3)Sc3ccccc3N4c3ccccc3)cc2)cc1
10-Phenyl-3-(2-{4′-[2-(10-phenylphenothiazin-3-yl)vinyl]biphenyl-4-yl}vinyl)phenothiazine

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他dried over molecular sieve
  2. 2
    workup.ADDITIONthe reaction solution was diluted with 200 ml of methanol
  3. 3
    workup.STIRRINGstirred for a further 15 min
  4. 4
    过滤The precipitate was filtered off
  5. 5
    洗涤washed with 500 ml of methanol
  6. 6
    其他dried at 35° C. under reduced pressure
  7. 7
    其他The crude product (5.85 g) was recrystallized in 400 ml of toluene
  8. 8
    其他were obtained

实验过程

2.73 g (24.1 mmol) of potassium tert-butoxide and then 7.80 g (25.7 mmol) of 10-phenylphenothiazine-3-carbaldehyde were added under nitrogen at room temperature with stirring to a solution of 4.83 g (10.7 mmol) of diethyl[4′-(diethoxyphosphorylmethyl)biphenyl-4-ylmethyl]phosphonate in 80 ml of dimethyl sulfoxide dried over molecular sieve. After stirring at room temperature for four hours, the reaction solution was diluted with 200 ml of methanol and stirred for a further 15 min. The precipitate was filtered off, washed with 500 ml of methanol and dried at 35° C. under reduced pressure. The crude product (5.85 g) was recrystallized in 400 ml of toluene. 3.85 g of yellow solid having a melting point of 278-290° C. were obtained.

来源

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