Réaction #2161223

ord-0392d3f1401547a6a41861c5b70333d3

Équation de réaction

C1=Cc2cc3ccc(cc4nc(cc5ccc(cc1n2)[nH]5)C=C4)[nH]3
porphyrin
c1cc[nH]c1
pyrrole
C[Si](C)(C)C#Cc1ccc(C=O)cc1
4-trimethylsilylethynylbenzaldehyde
CO
methanol
C[Si](C)(C)C#Cc1ccc(-c2c3nc(c(-c4ccc(C#C[Si](C)(C)C)cc4)c4ccc([nH]4)c(-c4ccc(C#C[Si](C)(C)C)cc4)c4nc(c(-c5ccc(C#C[Si](C)(C)C)cc5)c5ccc2[nH]5)C=C4)C=C3)cc1
porphyrin
Rendement 12.0%
C[Si](C)(C)C#Cc1ccc(-c2c3nc(c(-c4ccc(C#C[Si](C)(C)C)cc4)c4ccc([nH]4)c(-c4ccc(C#C[Si](C)(C)C)cc4)c4nc(c(-c5ccc(C#C[Si](C)(C)C)cc5)c5ccc2[nH]5)C=C4)C=C3)cc1
tetrakis(4-trimethylsilylethynylphenyl)porphyrin
Rendement 12.0%

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe temperature was subsequently increased
  2. 2
    Températureat reflux for 4 hours
  3. 3
    workup.WAITwas then left
  4. 4
    Autreto crystallize
  5. 5
    FiltrationThe medium was filtered over sintered glass
  6. 6
    Lavagethe product was rinsed with methanol

Mode opératoire

5.02 g of 4-trimethylsilylethynylbenzaldehyde (25 mmol) were dissolved in 210 ml of propionic acid and then heated to 80° C. 1.72 ml of pyrrole (25 mmol) were subsequently added portionwise over a period of one hour. The temperature was subsequently increased and the mixture was kept at reflux for 4 hours. After a return to ambient temperature, 75 ml of methanol were added to the reaction medium, which was then left to stand for 14 hours in order for the porphyrin to crystallize. The medium was filtered over sintered glass and the product was rinsed with methanol. 2.87 g (3 mmol; yield 12%) of the expected porphyrin (1) were obtained in the form of a purple powder.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07919046B2uspto-grants-2011_04