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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1986508Erstellt: 25. Oktober 2026

4-Nitrobenzaldehyde → 5-(4-Nitrophenyl)-1,3-oxazole

https://huagongshe.com/reaction/1986508

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzaldehydeHCID 541—
EduktSodium HydroxideHCID 14798—
EduktTosylmethyl isocyanideHCID 161915—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(4-Nitrophenyl)-1,3-oxazoleHCID 2737068144,8%

Reaktionsschritte

To an aqueous solution containing 0.84 g of sodium hydroxide were added 0.45 g of 4-nitrobenzaldehyde, 12.2 g of a methylene chloride solution containing 0.65 g of TosMIC which was obtained in the same way as that of Example 6 and 0.10 g of tetrabutyl ammonium bromide at room temperature. The mixture was allowed to react at room temperature until HPLC found no trace of the starting materials. Upon the completion of the reaction, the reaction solution was washed with water and dried over anhydrous magnesium sulfate. The solvents were distilled off. An HPLC analysis showed that the concentrated residue contained 0.82 g of the target compound (yield: 93%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE040795E1
Quelldatensatzuspto-grants-2009_06
ORD IDord-3650e42fe4904bae8e7195da84648b4e
Quellennotizuspto-grants-2009_06