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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075965Generated: October 31, 2026

Benzaldehyde → HCID 218198, compound

https://huagongshe.com/reaction/1075965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantImidazole, 1,5-dimethyl-2-nitro-HCID 78888—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthanolHCID 702—
ProductHCID 218198HCID 21819816%

Reaction Steps

A mixture of 7.2 g. of 1,5-dimethyl-2-nitroimidazole, 41.2 ml. of benzaldehyde and 7.9 g. of potassium tert-butoxide in 300 ml. of ethanol is refluxed for 35 minutes under nitrogen. The residue, which is obtained by evaporation of the reaction mixture under vacuum, is extracted with ethyl ether and filtered. The ethyl ether solution after concentration yields an oily residue which is chromatographed through 300 g. of silica gel by eluting with chloroform. After evaporation of the solvent under vacuum at 40° C., an oily residue is obtained which crystallizes on standing. After washing with a small amount of methyl ethyl ketone, 1.9 g. (16%) of a product which melts at 170°-180° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954789
Source datasetuspto-grants-1976_05
ORD IDord-bfe9f7e845df498097ac0436c398ff54
Source noteuspto-grants-1976_05