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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23519Erstellt: 23. Oktober 2026

Hydrochloric Acid → 1-(4-Fluorophenyl)-2-(2-fluoropyridin-4-yl)ethanone

https://huagongshe.com/de/reaction/23519

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
EduktBenzoic acid, 4-fluoro-, ethyl esterHCID 67976—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt2-Fluoro-4-methylpyridineHCID 2737403—
Produkt1-(4-Fluorophenyl)-2-(2-fluoropyridin-4-yl)ethanoneHCID 11031769—

Reaktionsschritte

To a solution of sodium bis(trimethylsilyl)amide (0.465 L, 1M) in TBF (765 mL) under nitrogen, cooled to 2° C., was added 2-fluoro-4-methylpyridine (25 g, 0.225 mol) and the solution stirred for 45 minutes in an ice bath. Ethyl 4-fluoro-benzoate (35 mL, 0.239 mol) was added and the reaction was stirred for 1.5 hours at RT. The reaction mixture was poured into excess aqueous 2N HCl, and the aqueous layer was made basic with 5 N NaOH and extracted with EtOAc. The organic extracts were combined, washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was dissolved in CH2Cl2 and filtered through a cotton plug. Hexanes were added and the CH2Cl2 was removed under reduced pressure until precipitation of the title compound occurred as a pale yellow solid (43.2 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852727B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-8b2ce258c09b4c8d8cddd43a27d5f774
Quellennotizuspto-grants-2005_02