Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2390121Erstellt: 24. Oktober 2026

Triethylamine → Tert-butyl{4-chloro-2-[(4-methylpyridin-3-yl)ethynyl]phenoxy}acetate

https://huagongshe.com/de/reaction/2390121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-Bromo-4-methylpyridineHCID 817630—
EduktTert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl{4-chloro-2-[(4-methylpyridin-3-yl)ethynyl]phenoxy}acetateHCID 58521948—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 3-bromo-4-methylpyridine (Apollo; 355 mg; 2.06 mmol), tert-butyl(4-chloro-2-ethynylphenoxy)acetate (Intermediate 3, 500 mg; 1.87 mmol), dichlorobis(triphenylphosphine)palladium(II) (82 mg; 0.11 mmol), copper(I) iodide (21 mg; 0.11 mmol) was degassed during two minutes under nitrogen then THF (7.5 mL) and triethylamine (520 μL; 3.75 mmol) were added and reaction mixture was stirred at 60° C. for 16 hours. The solvents were removed under vacuum affording a dark brown residue, which was purified by flash column chromatography (silica), eluting with cyclohexane containing increasing amounts of EtOAc. The title compound was obtained as a dark brown sticky solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08273769B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-8dfc4f7844f243e2a372e3758a0ac0ef
Quellennotizuspto-grants-2012_09