Reacción #487496

ord-2bfb35ad99f94463b0bf921b96521cff

Ecuación de reacción

O=C(O)c1ccc(-c2c3nc(c(-c4ccc(C(=O)O)cc4)c4ccc([nH]4)c(-c4ccc(C(=O)O)cc4)c4nc(c(-c5ccc(C(=O)O)cc5)c5ccc2[nH]5)C=C4)C=C3)cc1
tetra(4-carboxyphenyl)porphine
c1ccncc1
pyridine
CC(C)COC(=O)Cl
isobutyl chloroformate
C1=Cc2cc3ccc(cc4nc(cc5ccc(cc1n2)[nH]5)C=C4)[nH]3
Porphyrin

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe synthesis was performed in a three-necked flask under nitrogen
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.ADDITIONThe reaction mixture was mixed at 70° C. for 4 hours
  4. 4
    OtroThe product obtained
  5. 5
    Filtraciónwas filtered on a Buchner funnel with a sintered glass disc
  6. 6
    Lavadowashed with methanol till the transparent filtrate
  7. 7
    Otrowas obtained
  8. 8
    Otrothe product was dried in a vacuum dryer
  9. 9
    OtroA green powder was obtained

Procedimiento

The synthesis was performed in a three-necked flask under nitrogen. 50 mg of mezo-tetra(4-carboxyphenyl)porphine (4CP) was dissolved in 5 ml of dry DMSO, the catalysts, i.e. 120 μl of pyridine and 30 μl of isobutyl chloroformate, were added and after 5 minutes a suspension of 0.5 g Cloisite 30 B in 15 ml of dry DMSO was added. The reaction mixture was mixed at 70° C. for 4 hours. The product obtained was filtered on a Buchner funnel with a sintered glass disc and washed with methanol till the transparent filtrate was obtained and then the product was dried in a vacuum dryer. A green powder was obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08741156B2uspto-grants-2014_06