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HRID 352079Erstellt: 24. Oktober 2026

Toluene → 4-(hydroxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole

https://huagongshe.com/de/reaction/352079

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Edukt1,3-DichloroacetoneHCID 10793—
EduktPotassium CarbonateHCID 11430—
Edukt4-(Trifluoromethyl)cinnamamideHCID 5709014—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(hydroxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazoleHCID 1299284762%

Reaktionsschritte

(E)-3-(4-(Trifluoromethyl)phenyl)-2-propenamide (4.30 g, 20.0 mmol) and 1,3-dichloroacetone (4.75 g, 37.4 mmol) were added to toluene (20 ml) and the mixture was subjected to refluxing azeotropic dehydration using a Dean-Stark tube for 6 hours. The reaction mixture was allowed to cool to room temperature, and DMF (50 ml), water (30 ml) and potassium carbonate (13.7 g, 99.1 mmol) were added. The mixture was stirred at 100° C. for 1.5 hours. After allowing to cool to room temperature, ethyl acetate (200 ml) and water (150 ml) were added and the mixture was partitioned. The organic layer was washed with water/saturated brine (1:1, 100 ml). To the organic layer was added ethyl acetate (400 ml), and the mixture was washed with water (200 ml) twice and concentrated under reduced pressure. Ethanol (30 ml) was added to the residue. Water (38 ml) was added and the precipitated crystals were collected by filtration, washed with water (40 ml) and dried under reduced pressure to give 4-(hydroxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole (3.3 g, 3.71 mmol, yield 62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743924B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-0a8d5c38ed564c68853174856e713334
Quellennotizuspto-grants-2004_06