HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65544Generated: October 29, 2026
Benzaldehyde → HCID 135446084, compound
https://huagongshe.com/reaction/65544
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Pyrrole | HCID 8027 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Solvent | Propionic Acid | HCID 1032 | — |
| Product | HCID 135446084 | HCID 135446084 | — |
Reaction Steps
15.2 ml of benzaldehyde and 7.51 g of 4-carboxybenzaldehyde are dissolved in 746 ml of boiling propionic acid, treated dropwise with 13.9 ml of pyrrole, the mixture obtained is subsequently heated under reflux for about 30 minutes and then left to cool to room temperature. The porphine derivative is precipitated by the addition of 0.5 l of water. The filtered-off crude product is pre-purified by two-fold column chromatography on 1.2 kg of silica gel, in each case the elution being carried out with the following solvents in sequence: chloroform/cyclohexane (1:1), chloroform/ethyl acetate (3:2) and (1:1), ethyl acetate and ethyl acetate which contains 2% methanol. For the further purification, the product is suspended in a small amount of methanol and filtered off. This procedure is repeated until the filtrate is only faintly coloured. The thus-obtained product is then chromatographed on a silica gel column using chloroform, chloroform/ethyl acetate (1:1) and ethyl acetate as the elution agent. There are obtained 1.7 g of 4-(10,15,20-triphenyl-21H,23H-porphin- 5-yl)benzoic acid as violet crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04614723 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-431b0cdb38e74b3ca50046a77ca95cf3 |
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| Source note | uspto-grants-1986_09 |
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