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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2390106Erstellt: 24. Oktober 2026

Ethyl Acetate → Tert-butyl(4-chloro-2-ethynylphenoxy)acetate

https://huagongshe.com/de/reaction/2390106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktTetrabutylammonium Fluoride TrihydrateHCID 11726816—
EduktTert-butyl{4-chloro-2-[(trimethylsilyl)ethynyl]phenoxy}acetateHCID 56594380—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—

Reaktionsschritte

A solution of tert-butyl{4-chloro-2-[(trimethylsilyl)ethynyl]phenoxy}acetate (Intermediate 2, 17.70 g; 52.2 mmol) in THF (180 mL) was treated with tetrabutylammonium fluoride trihydrate (16.48 g; 52.2 mmol). The reaction mixture was stirred for 4 hours, then ethyl acetate (450 mL) was added and the organic phase was washed with water (750 mL) then with brine (750 mL), dried over MgSO4, filtered and concentrated under vacuum to give a brown oily residue which was purified by flash chromatography (silica) eluting with cyclohexane containing increasing amounts of ethyl acetate. The title compound was obtained as a brown oil which solidified after prolonged standing.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08273769B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-b18812189ce24d5c8731b2516ed810b4
Quellennotizuspto-grants-2012_09