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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118950Generated: October 28, 2026

4-Nitrobenzaldehyde → HCID 53983876, compound

https://huagongshe.com/reaction/2118950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-MethylpyrimidineHCID 18922—
SolventWaterHCID 962—
ProductHCID 53983876HCID 5398387677%

Reaction Conditions

Temperature120 °C

Reaction Steps

The starting compound is prepared as follows. p-Nitrobenzaldehyde (24.2 g), 4-methyl-pyrimidine (15.5 g) and acetic anhydride (16.7 g) are mixed at room temperature, and the mixture is heated at 120° C. for 5 hours. After cooling, the mixture is poured into water (500 ml), and the aqueous mixture is extracted several times with chloroform. The combined chloroform extracts are dried over magnesium sulfate and concentrated until crystals separated. Addition of ether gives 4-[2-(p-nitrophenyl)ethenyl]pyrimidine (28 g), m.p. 213°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04681884
Source datasetuspto-grants-1987_07
ORD IDord-384f58d0299f4858a983b6baee5b5b37
Source noteuspto-grants-1987_07