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HRID 339127Erstellt: 24. Oktober 2026

Benzene, 1-iodo-3-(trifluoromethyl)- → 2,2-Difluoro-1-[3-(trifluoromethyl)phenyl]-1-propanone

https://huagongshe.com/de/reaction/339127

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 1-iodo-3-(trifluoromethyl)-HCID 67868—
Edukt2,2-difluoro-N-methoxy-N-methylpropanamideHCID 58736313—
EduktHCID 178418918HCID 178418918—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,2-Difluoro-1-[3-(trifluoromethyl)phenyl]-1-propanoneHCID 58247996—

Reaktionsbedingungen

Temperatur-15 °C

Reaktionsschritte

A solution of 2-propylmagnesium chloride in THF (1.3 M, 7.5 ml) was cooled to −15° C. and admixed with 1-iodo-3-(trifluoromethyl)benzene (2.80 g, 10.2 mmol). The reaction mixture was stirred at −15° C. for 1 h, warmed to room temperature and admixed dropwise with a solution of 2,2-difluoro-N-methoxy-N-methylpropanamide (1.43 g, 9.35 mmol; prepared according to Synth. Comm. 2008 (38), 1940-1945), and stirred at room temperature overnight. Then the mixture was added to ice-cold dilute hydrochloric acid and extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by means of silica gel chromatography with the eluent cyclohexane/ethyl acetate (EA) (0% EA to 30% EA).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889878B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-dcbaa6e30ea6492190224c0783530890
Quellennotizuspto-grants-2014_11