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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65544Generated: October 29, 2026

Benzaldehyde → HCID 135446084, compound

https://huagongshe.com/reaction/65544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPyrroleHCID 8027—
Reactant4-Formylbenzoic acidHCID 12088—
SolventPropionic AcidHCID 1032—
ProductHCID 135446084HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614723
Source datasetuspto-grants-1986_09
ORD IDord-431b0cdb38e74b3ca50046a77ca95cf3
Source noteuspto-grants-1986_09