Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Myristyl bromide | HCID 8208 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin | HCID 135438030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136049179 | HCID 136049179 | — |
Reaction Steps
5,10,15,20-tetrakis-(4-Hydroxy-phenyl)-porphyrin (170 mg, 0.25 mmol) is dissolved and K2CO3 (0.65 g, mmol) is suspended in DMF (30 mL). To the vigorously stirred reaction mixture a solution of 1-bromotetradecane (0.1 mL, 0.45 mmol) in DMF (10 mL) is added dropwise at 50° C. during 30 mins and the mixture is heated for 1.5 h. After evaporation of solvent, the residue is dissolved in toluene:ethanol (1:1 by vol., ca. 5 mL) and purified by chromatography using a column (5×25 cm) of silica gel (Merck 60) which is washed with toluene. After the elution of the first 3 fractions, elution is continued using toluene:ethyl acetate (2:1 by vol.). The fifth compound eluted is collected, the solvent evaporated and the residue dried under high vacuum to afford product as a violet solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977474B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-7587a7284ee14feb9f584c478087f935 |
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| Source note | uspto-grants-2011_07 |
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