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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 523042Erstellt: 25. Oktober 2026

N-bromobutanimide → HCID 178470399, Verbindung

https://huagongshe.com/reaction/523042

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
EduktEthyl 4(5)-imidazolecarboxylateHCID 99170—
LösungsmittelAcetonitrileHCID 6342—
ProduktHCID 178470399HCID 178470399—

Reaktionsschritte

NBS (25 g, 140 mmol) is added to a stirred solution of ethyl 3H-imidazole-4-carboxylate (I-17) in 1.4 L of MeCN. The reaction mixture is stirred for 12 h in the dark, then is concentrated and purified by silica chromatography (0-70% EtOAc in heptane) to provide 17 g (65 mmol) of ethyl 3H-imidazole-4-carboxylate ethyl 4-bromo-1H-imidazole-5-carboxylate (I-18) as a white solid. This material is stirred with 11 g (78 mmol) of K2CO3 and 8.5 mL (71 mmol) of benzyl bromide in 200 mL of DMF for 12 h. The reaction is diluted with water and extracted with three times with EtOAc. Extracts are combined, washed with brine, dried over Na2SO4, filtered, concentrated and purified via silica chromatography (0-50% EtOAc in heptane) to provide 9.6 g (31 mmol) of ethyl 3-benzyl-5-bromo-imidazole-4-carboxylate (I-19) as a colorless oil that solidified upon standing.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09334285B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-6f9834d4244a4299a27c518716e7e373
Quellennotizuspto-grants-2016_05