HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074041Generated: October 30, 2026
Methanol → 5,10,15,20-Tetrakis[4-[2-(trimethylsilyl)ethynyl]phenyl]-21H,23H-porphine
https://huagongshe.com/reaction/2074041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyrrole | HCID 8027 | — |
| Reactant | 4-(Trimethylsilylethynyl)benzaldehyde | HCID 2771643 | — |
| Reactant | 21H,22H-Porphine | HCID 137705241 | — |
| Solvent | Propionic Acid | HCID 1032 | — |
| Product | 5,10,15,20-Tetrakis[4-[2-(trimethylsilyl)ethynyl]phenyl]-21H,23H-porphine | HCID 135475294 | 12% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919046B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-0392d3f1401547a6a41861c5b70333d3 |
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| Source note | uspto-grants-2011_04 |
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