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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76892Erstellt: 23. Oktober 2026

2-Bromobenzyl bromide → 3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]propionic acid methyl ester

https://huagongshe.com/de/reaction/76892

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromobenzyl bromideHCID 76965—
EduktMethyl 3-(1-Tritylimidazol-4-yl) PropionateHCID 10475868—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]propionic acid methyl esterHCID 58827130—

Reaktionsschritte

To a solution of 3-(1-trityl-1H-imidazol-4-yl)propanoic acid methyl ester (5.0 g, 12.6 mmol) in CH3CN (80 mL) is added a solution of 2-bromobenzylbromide (2.84 g, 11.4 mmol) in CH3CN (20 mL). The resulting clear solution is stirred at ambient temperature over the weekend. The mixture is concentrated and the remaining oil is taken up in 85 mL methanol and heated up at 70° C. for 2 h. Then the mixture is concentrated to give a yellow oil, which is taken up in EtOAc and washed with saturated aqueous NaHCO3 and brine, dried over anhydrous Na2SO4, and concentrated to yield a viscous oil. The crude reaction mixture is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to give the desired compound. MS (ESI) m/z 323 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835646B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-b41e2132a9a845cb9b032efa260435e5
Quellennotizuspto-grants-2014_09