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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232275Generated: October 31, 2026

4-Nitrobenzaldehyde → HCID 53983876, compound

https://huagongshe.com/reaction/2232275

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 numberUS04788198
Source datasetuspto-grants-1988_11
ORD IDord-f12d688328ba4aeda8f1ca6b729b0d18
Source noteuspto-grants-1988_11