Réaction #1747865

ord-38520b3f6dcc4101ad9f5fcda4cd91a1

Équation de réaction

Cl
hydrochloric acid
O=C(Cl)c1ccccc1
benzoyl chloride
Oc1ccccc1N1c2ccccc2Sc2ccccc21
10-(2-hydroxyphenyl)phenothiazine
O=C(Oc1ccccc1N1c2ccccc2Sc2ccccc21)c1ccccc1
2-(Phenothiazin-10-yl)phenyl benzoate

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe reaction solution was heated to 60-65° C.
  2. 2
    workup.STIRRINGstirred at this temperature for 15 min
  3. 3
    TempératureAfter cooling to room temperature
  4. 4
    workup.STIRRINGthe suspension was then stirred overnight
  5. 5
    workup.STIRRINGstirred for 1 h
  6. 6
    FiltrationThe suspension was filtered through a glass frit
  7. 7
    LavageThe residue was washed
  8. 8
    Autredried at 60° C. under reduced pressure
  9. 9
    Autrewere obtained

Mode opératoire

16.0 g (114 mmol) of benzoyl chloride were added dropwise at 0-5° C. with stirring to a solution of 4.00 g (13.7 mmol) of 10-(2-hydroxyphenyl)phenothiazine in 24 ml of pyridine within 30 min. After stirring at room temperature for 2 h, the reaction solution was heated to 60-65° C. and stirred at this temperature for 15 min. After cooling to room temperature, the suspension was then stirred overnight. After adding 300 ml of ice-water, the suspension was admixed slowly with 19 ml of conc. hydrochloric acid (pH 0.9) and stirred for 1 h. The suspension was filtered through a glass frit. The residue was washed to neutrality with 2 l of water and dried at 60° C. under reduced pressure. 2.87 g (53% of theory) of colorless microcrystals having a melting point of 144-148° C. were obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08029919B2uspto-grants-2011_10