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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20200Generated: October 26, 2026

5-((1H-Pyrrol-2-YL)methyl)-1H-pyrrole-2-carbaldehyde → Dipyrromethane

https://huagongshe.com/reaction/20200

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-((1H-Pyrrol-2-YL)methyl)-1H-pyrrole-2-carbaldehydeHCID 16732691—
Reactant21H,22H-PorphineHCID 137705241—
ProductDipyrromethaneHCID 14081446%

Reaction Steps

1-Formyldipyrromethane 2 is the key precursor for the porphine synthesis described herein. Formylation of dipyrromethane via Vilsmeier or Grignard reagent mediated syntheses21 results in multiple byproducts, requiring tedious chromatographic separation for the purification of 1-formyldipyrromethane (2). The TLC and 1H NMR analyses of the crude reaction mixture obtained from Vilsmeier formylation of dipyrromethane showed the presence of three components: starting dipyrromethane (3), 1-formyldipyrromethane (2), 1,9-diformyldipyrromethane (4), and an unknown byproduct (tentatively assigned as a 2-formyldipyrromethane) in a ratio of 7:20:4:1. We were able to separate the desired 2 in 46% yield (without using a tin complexation strategy); however, the purification required lengthy column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745618B2
Source datasetuspto-grants-2010_06
ORD IDord-1ae614c9e1c44c79a850d45cef6482db
Source noteuspto-grants-2010_06