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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Butyl-5-chloro-3-(4-nitro-benzyl)-3h-imidazole-4-carbaldehyde | HCID 19815397 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Benzyltriphenylphosphonium chloride | HCID 70671 | — |
| Product | 1-(4-Nitrobenzyl)-2-butyl-4-chloro-5-(2-phenylethen-1-yl)imidazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155118 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-cafd2a79c97a4f07b56c5d0c2654f7c1 |
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| Source note | uspto-grants-1992_10 |
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