Salicylaldehyde → 5,10,15,20-tetra(2-hydroxyphenyl)porphyrin

HRID 1059487Notes

Reaction equation

HRID 1059487 reaction equation
[NH:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[CH:6](=O)[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9]>C(O)(=O)CC>[OH:9][C:8]1[CH:10]=[CH:11][CH:12]=[CH:13][C:7]=1[C:6]1[C:5]2[NH:1][C:2]([C:6]([C:7]3[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=3[OH:9])=[C:2]3[N:1]=[C:5]([C:6]([C:7]4[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=4[OH:9])=[C:2]4[NH:1][C:5](=[C:6]([C:7]5[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=5[OH:9])[C:2]5[CH:3]=[CH:4][C:5]=1[N:1]=5)[CH:4]=[CH:3]4)[CH:4]=[CH:3]3)=[CH:3][CH:4]=2

Participants

4

Reactant 2

HCID 6998SalicylaldehydeHCID 8027Pyrrole

Product 1

HCID 1354748445,10,15,20-tetra(2-hydroxyphenyl)porphyrin

Reagents, catalysts & solvents 1

HCID 1032Propionic AcidSolvent

Procedure

Pyrrole (1.0 equivalents) and salicylaldehyde (1.2 equivalents) are dissolved in propionic acid (1 liter/20 ml pyrrole) and the solution is refluxed for 30 minutes. The reaction mixture is allowed to cool to room temperature and stand for one day. The mixture is filtered and the product is recrystallized to yield 5,10,15,20-tetrakis(2′-hydroxyphenyl) porphyrin.

Workup

  1. temperaturethe solution is refluxed for 30 minutes
  2. filtrationThe mixture is filtered
  3. customthe product is recrystallized

Sources & evidence

ORD record
ord-2ea0399337ea4c16b83ff5feec6d7f90
Source dataset
uspto-grants-2003_02
Patent number
US06521561B1

Reaction notes

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