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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043325Generated: November 4, 2026

1H-Imidazole-4-carbaldehyde → HCID 59728050, compound

https://huagongshe.com/reaction/2043325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 28440728HCID 28440728—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 59728050HCID 5972805049%

Reaction Conditions

Temperature40 °C

Reaction Steps

N-Isopropyl-3-chloro-4-methoxy-aniline (0.20 g, 1.0 mmol) was dissolved in methanol (10 ml). Then 4-formylimidazole (0.288 g, 3.0 mmol) and zinc chloride (0.545 g, 4.0 mmol) were added and the reaction mixture was cooled with an ice bath. After adding sodium cyanoborohydride (0.189 g, 3.0 mmol) the mixture was allowed to stir at 40° C. overnight. After cooling, the reaction mixture was poured onto ammoniumchloride/ice and extracted with ethyl acetate (3 times 20 ml). The organic layer was dried over magnesium sulfate and evaporated. The residue was purified using flash chromatography (column: Isolute® Flash-NH2 (Separtis); eluent: ethyl acetate/methanol=95:5) to yield a white solid (136 mg, 49%); MS (ISP): 280.0 ((M+H)+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586617B2
Source datasetuspto-grants-2013_11
ORD IDord-5788b6360c3646eea2226f33806f7a4a
Source noteuspto-grants-2013_11