HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 466445Erstellt: 24. Oktober 2026
Benzene → 3-[2-Butyl-4-chloro-1-(4-nitrobenzyl)imidazol-5-yl]propenoic acid ethyl ester
https://huagongshe.com/de/reaction/466445
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzene | HCID 241 | — |
| Edukt | Carboxymethylene triphenylphosphorane | HCID 10870911 | — |
| Edukt | 2-Butyl-5-chloro-3-(4-nitro-benzyl)-3h-imidazole-4-carbaldehyde | HCID 19815397 | — |
| Produkt | 3-[2-Butyl-4-chloro-1-(4-nitrobenzyl)imidazol-5-yl]propenoic acid ethyl ester | HCID 53660932 | — |
Reaktionsschritte
A mixture of 1.2 g of 1-(4-nitrobenzyl)-2-butyl-4-chloroimidazole-5-aldehyde and 1.5 g of (carboxymethylene)triphenylphosphorane in 50 mL of benzene was refluxed for 2 hours. The reaction mixture was concentrated and the residue was purified by flash column chromatography on silica gel (Hexane: EtOAc=3:1 elution). The major product, the E isomer, was eluted first and was obtained as a thick oil initially which solidified to give an amorphous solid, 1.2 g. The minor product, the Z isomer was eluted next and was isolated as a thick liquid, 85 mg. E isomer: NMR (200 MHz, CDCl3): 7.3 and 6.53 (d, 2H, 5=16 Hz); 5.3 (s, 2H); 2.62 (t, 2H, J=7.3 Hz); 1.69 (m, 2H); 1.28 (m, 5H); 0.89 (t, 3H, J=7.3 Hz). Z isomer: NMR (200 MHz, CDCl3): (key peaks only) δ 6.45 and 6.02 (d, 2H, J=11.8 Hz); 5.17 (s, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05155118 |
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| Quelldatensatz | uspto-grants-1992_10 |
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| ORD ID | ord-5d810c67ce6f4ec7963267689a5925eb |
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| Quellennotiz | uspto-grants-1992_10 |
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