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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2086625Erstellt: 27. Oktober 2026

Ethyl trifluoroacetate → Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-

https://huagongshe.com/reaction/2086625

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl trifluoroacetateHCID 9794—
EduktHexamethyldisilazaneHCID 13838—
Edukt1-(4-(1H-Imidazol-1-yl)phenyl)ethanoneHCID 82316—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktButane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-HCID 6426099—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a THF (5 mL) solution of 1,1,1,3,3,3-hexamethyldisilazane (0.178 g, 1.1 mmol) was added n-butyl lithum (1.6 M solution in hexane, 0.72 mL, 1.2 mmol) at 0° C. under nitrogen, and the mixture was stirred for 30 minutes, and cooled to −78° C. 4-(1-Imidazolyl)acetophenone (prepared according the method of M. A. Khan et. al., J. Chem. Soc. C., 1970, 85., 0.186 g, 1.0 mmol) was added to the mixture, and residue was stirred for 1 hour. Ethyl trifluoroacetate (0.17 g, 1.2 mmol) was added tothe reaction mixture, the residure was warm to room temperature. The reaction mixture was poured into ice water and the whole was extracted with ethyl acetate (30 mL×2). The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The resulting solid was washed with small amount of ethyl acetate to give the title compound (0.163 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06727238B2
Quelldatensatzuspto-grants-2004_04
ORD IDord-47d82a0ad86849989e5f6b0d15c3c62a
Quellennotizuspto-grants-2004_04