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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722772Generated: October 25, 2026

1-Phenyl-2-buten-1-one → Methyl 4-methyl-2-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylate

https://huagongshe.com/reaction/1722772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-2-buten-1-oneHCID 71090—
ReactantMethyl 3-amino-3-(3-nitrophenyl)prop-2-enoateHCID 69855994—
Solvent1-ButanolHCID 263—
ProductMethyl 4-methyl-2-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylateHCID 100663225.8%

Reaction Steps

A mixture of methyl 3-amino-3-(3-nitrophenyl)acrylate (45 g) and 1-phenyl-2-buten-1-one (44 g) in n-butanol (450 ml) was refluxed for 4 hours. After allowing to cool at ambient temperature, the reaction mixture was evaporated in vacuo. The residue was subjected to a column chromatography on silica gel (500 g) eluting with benzene. The fractions containing the object compound were combined and concentrated under reduced pressure to give methyl 4-methyl-2-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylate (4.10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857527
Source datasetuspto-grants-1989_08
ORD IDord-4d0c56193547477cbd348e812bd578f2
Source noteuspto-grants-1989_08