Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1440124Erstellt: 26. Oktober 2026

Acetic Acid → 4-(2,4-Difluorophenyl)-1,1,1-trifluoro-4-hydroxy-3-buten-2-one

https://huagongshe.com/reaction/1440124

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktMethanolHCID 887—
EduktEthyl trifluoroacetateHCID 9794—
Edukt2,4-DifluoroacetophenoneHCID 67770—
EduktSodium MethoxideHCID 10942334—
LösungsmittelDiethyl EtherHCID 3283—
Produkt4-(2,4-Difluorophenyl)-1,1,1-trifluoro-4-hydroxy-3-buten-2-oneHCID 6993477897,4%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of 40.0 g (0.256 moles) 2',4'-difluoroacetophenone (commercially available) in 400 mL diethyl ether at 0° C. was added 40 mL (0.405 moles) ethyl trifluoroacetate. At 5° C., 80 mL of a 25% wt. sodium methoxide in methanol (0.37 moles) were added over 15 minutes. The reaction mixture was stirred overnight at 25° C. The mixture was poured over 300 mL ice water and 21.3 mL (0.37 moles) acetic acid were added. The organic layer was washed two times with water, dried over anhydrous MgSO4, and concentrated in vacuo to give 62.85 g (97%) 4-(2,4-difluorophenyl)-1,1,1-trifluoro-4-hydroxy-3-buten-2-one as a yellow oil; 1HNMR (CDCl3) ppm: 6.61 (s,1H), 6.87 (m, 1H)., 6.97 (m, 1H), 7.97 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05496956
Quelldatensatzuspto-grants-1996_03
ORD IDord-ce1c43850534496baa6781f7002c1305
Quellennotizuspto-grants-1996_03