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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873763Erstellt: 26. Oktober 2026

2-Bromo-1-(4-fluorophenyl)ethan-1-one → 4-(4-Fluorophenyl)-1,3-thiazole-2-carbaldehyde

https://huagongshe.com/reaction/1873763

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-1-(4-fluorophenyl)ethan-1-oneHCID 96749—
Edukt2,2-DiethoxythioacetamideHCID 2794734—
LösungsmittelEthanolHCID 702—
Produkt4-(4-Fluorophenyl)-1,3-thiazole-2-carbaldehydeHCID 3704005—

Reaktionsschritte

5 g (23.04 mmol) of 4-fluorophenacyl bromide and 3.76 g (23.04 mmol) of 2,2-diethoxythioacetamide in 100 ml of ethanol were stirred at room temperature for 2 h. After concentration, the residue was treated with ethyl acetate and filtered. The filtrate was concentrated and the obtained residue, which consisted of the diethyl acetal of 4-(4-fluoro-phenyl)-thiazole-2-carbaldehyde, was treated with 100 ml of acetone/water and 1 ml of 2 N hydrochloric acid. After stirring at room temperature for 2 h, the reaction mixture was evaporated. Yield: 4.22 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304438B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-4139f95737654de687d379e05b7df272
Quellennotizuspto-grants-2012_11