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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371963Generated: October 29, 2026

2,5-Hexanedione → 4-(2,5-Dimethyl-1H-pyrrol-1-yl)benzaldehyde

https://huagongshe.com/reaction/2371963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-HexanedioneHCID 8035—
Reactant4-AminobenzaldehydeHCID 11158—
ReactantHCID 86745551HCID 86745551—
Product4-(2,5-Dimethyl-1H-pyrrol-1-yl)benzaldehydeHCID 2764550—

Reaction Steps

Similarly prepared is N-acetyl-N-acetyloxy-[4-(2,5-dimethyl-1H-pyrrol-1-yl)-cinnamylamine. The starting material is prepared by first condensing p-amino-benzaldehyde with acetonylacetone to obtain 4-(2,5-di-methyl-1H-pyrrol-1-yl)-benzaldehyde which is in turn condensed with diethyl phosphonoacetaldehyde diethylacetal to obtain 4-(2,5-dimethyl-1H-pyrrol-1-yl)-cinnamaldehyde. The aldehyde is then converted to the oxime and reduced to the hydroxylamine according to previously described procedures.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05096919
Source datasetuspto-grants-1992_03
ORD IDord-d3a8c64b060b446c8f7641059b17090b
Source noteuspto-grants-1992_03