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HRID 260941Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/260941

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
PatentnummerUS05530126
Quelldatensatzuspto-grants-1996_06
ORD IDord-93fec1efbcf14b1584fc947bce38242c
Quellennotizuspto-grants-1996_06