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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45272Erstellt: 24. Oktober 2026

Urea → Benzenepropanal

https://huagongshe.com/de/reaction/45272

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktUreaHCID 1176—
Edukt2-Bromo-3-phenylpropanalHCID 11390228—
Edukt5-Benzyloxazol-2-amineHCID 60027526—
LösungsmittelEthanolHCID 702—
ProduktBenzenepropanalHCID 7707—

Reaktionsschritte

5-Benzyl-oxazol-2-ylamine A mixture of 2-bromo-3-phenylpropionaldehyde (14.2 g, crude from above) and urea (7.2 g, 0.12 mol) were heated at reflux for 15 hours in 200 mL of ethanol. The solvent was evaporated to dryness and the residue was diluted with dichloromethane (250 mL) and then washed with sodium hydroxide (10% aqueous solution, 100 mL) and water (50 mL). The organic layer was washed three times with hydrochloric acid (5% aqueous solution, 250 mL). The combined aqueous layers were brought to pH 9 to 10 with a 10% aqueous solution of sodium hydroxide and then extracted three times with dichloromethane (300 mL). The organic layer was dried over sodium sulfate, evaporated to dryness, and purified by silica gel column chromatography to give a pale yellow solid (1.6 g, 9.2 mmol, 9.2% from 3-phenyl-propionaldehyde). ESI-MS m/z calc. 174.1. found 175.1 (M+1)+; 1H NMR (CDCl3) δ 7.32-7.22 (m, 5H), 6.39 (s, 1H), 4.72 (bs, 2H), 3.84 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541453B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-a7cd14ff2615466eafaf4d5b09a4529c
Quellennotizuspto-grants-2013_09