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HRID 129207Erstellt: 23. Oktober 2026

Hydrochloric Acid → 4,4-Difluoro-1-[4-(morpholino)phenyl]-butane-1,3-dione

https://huagongshe.com/de/reaction/129207

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl difluoroacetateHCID 9961—
Edukt4-MorpholinoacetophenoneHCID 38362—
EduktSodium MethoxideHCID 10942334—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4,4-Difluoro-1-[4-(morpholino)phenyl]-butane-1,3-dioneHCID 1892037591,6%

Reaktionsschritte

Ethyl difluoroacetate (2.30 g, 18.5 mmol) was placed in a 100 mL round bottom flask and dissolved in THF (25 mL). To the stirred solution was added 25 weight % sodium methoxide (4.90 g, 22.6 mmol) followed by 4'-morpholinoacetophenone (3.45 g, 16.8 mmol). The reaction was stirred at room temperature overnight (15.8 hours), then treated with 3N HCl (13 mL). The reaction was extracted with ethyl acetate (20 mL), washed with brine (20 mL), dried over MgSO4, and concentrated in vacuo to give a green solid (4.36 g) which was recrystallized from methylene chloride/isooctane to give the diketone as a yellow solid (3.27 g, mp 102°-3° C., 69%). 1H NMR (CDCl3) 300 MHz 15.80 (br s, 1H), 7.86 (d, J=9.1 Hz, 2H), 6.90 (d, J=9.1 Hz 2H), 6.46 (s, 1H), 5.99 (t, J=54.4 Hz, 1H), 3.84 (m,4H), 3.36 (m, 4H); 19F NMR (CDCl3) 300 MHz: -126.75 (d); M+283.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05466823
Quelldatensatzuspto-grants-1995_11
ORD IDord-c140a6e036c340d58d3000033e28f887
Quellennotizuspto-grants-1995_11