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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466451Generated: October 25, 2026

Tetrahydrofuran → 1-(4-Nitrobenzyl)-2-butyl-4-chloro-5-(2-phenylethen-1-yl)imidazole

https://huagongshe.com/reaction/466451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Butyl-5-chloro-3-(4-nitro-benzyl)-3h-imidazole-4-carbaldehydeHCID 19815397—
ReactantButyllithiumHCID 178418339—
CatalystBenzyltriphenylphosphonium chlorideHCID 70671—
Product1-(4-Nitrobenzyl)-2-butyl-4-chloro-5-(2-phenylethen-1-yl)imidazoleHCID 54113661—

Reaction Steps

A solution of 0.4 g of benzyltriphenylphosphonium chloride in 20 mL of dried THF was cooled to -30°. To the above solution was added 0.65 mL of 1.6M n-BuLi dropwise. As the BuLi was added the solution turned to deep orange color. After stirring for 10 min. at -30°, 0.32 g of 1-(4-nitrobenzyl)-2-butyl-4-chloroimidazole-5-aldehyde was added and the reaction mixture was allowed to warm up to room temperature and stirred at room temperature for 2 hours. The reaction mixture was quenched with 2 mL of saturated NH4Cl solution and diluted with ethyl acetate, and the ethyl acetate solution was washed with water and a brine solution. Evaporation gave a thick oily residue which was purified by the flash silica gel column chromatography (hexane:ethyl acetate=3:1 elution) to give a thick yellow oil, 0.39 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155118
Source datasetuspto-grants-1992_10
ORD IDord-cafd2a79c97a4f07b56c5d0c2654f7c1
Source noteuspto-grants-1992_10