Reacción #2460328

ord-4160a45f63744d99a0b8e64e53335438

Ecuación de reacción

CCCCc1ccc(N2c3ccccc3Sc3ccccc32)cc1
10-(4-butylphenyl)-10H-phenothiazine
F[P-](F)(F)(F)(F)F.c1ccc([I+]c2ccccc2)cc1
diphenyliodonium hexafluorophosphate
CCCCc1ccc(N2c3ccccc3[S+](c3ccccc3)c3ccccc32)cc1.F[P-](F)(F)(F)(F)F
10-(4-butylphenyl)-5-phenyl-10H-phenothiazin-5-ium hexa-fluorophosphate

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaUpon cooling to ambient temperature
  2. 2
    workup.ADDITIONwas added
  3. 3
    Lavadowashed with ether
  4. 4
    Filtracióncollected by filtration
  5. 5
    Lavadowashed three times with ether
  6. 6
    OtroWithout further purification
  7. 7
    Otroit was isolated in 98.2% (2.36 g)
  8. 8
    Otroyield as a pale yellow solid

Procedimiento

A mixture of 10-(4-butylphenyl)-10H-phenothiazine (83) (1.44 g, 4.34 mmol), diphenyliodonium hexafluorophosphate (1.85 g, 4.34 mmol) and copper (I) benzoate (0.10 g) was heated at 120° C. for 3 hours under nitrogen. Upon cooling to ambient temperature, the mixture was transferred to a mortar-and-pestle and 50 ml of ether was added. The solid was finely powdered, washed with ether, collected by filtration and washed three times with ether. Without further purification, it was isolated in 98.2% (2.36 g) yield as a pale yellow solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07459106B2uspto-grants-2008_12