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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 474113Erstellt: 24. Oktober 2026

Ethyl difluoroacetate → 1-(6-Bromo-3-fluoro-4-(triethylsilyl)pyridin-2-yl)-2,2-difluoroethanone

https://huagongshe.com/reaction/474113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl difluoroacetateHCID 9961—
EduktLithium diisopropylamideHCID 2724682—
Edukt2-Bromo-5-fluoro-4-(triethylsilyl)pyridineHCID 86668068—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(6-Bromo-3-fluoro-4-(triethylsilyl)pyridin-2-yl)-2,2-difluoroethanoneHCID 8666808375%

Reaktionsschritte

To a freshly prepared solution of LDA (6.25 mmol) in THF (5 ml) was added dropwise a solution of 2-bromo-5-fluoro-4-triethylsilanylpyridine (1.6 g, 5.51 mmol) in THF (12 ml) at −78° C. Stirring was continued at −78° C. for 3 hours. Ethyl 2,2-difluoroacetate (0.58 ml, 5.51 mmol) was added dropwise and the solution was stirred at −78° C. for 3 hours. The reaction mixture was quenched with sat. ammonium chloride solution (20 ml) and ethyl acetate was added. The organic phase was washed with brine, dried over sodium sulfate, filtered and evaporated. The crude brown oil (2.11 g) was chromatographed over silica gel (cyclohexane/ethyl acetate) to give the title compound. 1.53 g (75% yield, mixture of ketone and hydrate form).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637508B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-8af69c0d2e084b30878654b5c5d26b4b
Quellennotizuspto-grants-2014_01