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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19783Erstellt: 24. Oktober 2026

Ammonium Chloride → 2-Chloro-4-ethynylpyridine

https://huagongshe.com/de/reaction/19783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktTetrabutylammonium FluorideHCID 2724141—
Edukt2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridineHCID 21985391—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Chloro-4-ethynylpyridineHCID 2343683191,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2.389 g of 2-chloro-4-trimethylsilanylethynyl-pyridine (11.39 mmol) in THF (90 ml) were added 11.39 ml of a 1 M TBAF solution in THF at −78° C. and the reaction mixture was stirred for 45 min at 0° C. Then saturated NH4Cl solution was added and the THF was removed under reduced pressure. The aqueous mixture was extracted with diethylether and the combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and concentrated in vacuo. The remaining residue was purified by column chromatography (pentane/diethylether 100:0 to 4:1) to give 2-chloro-4-ethynyl-pyridine (1.427 g, 91%) as an off-white solid. 1H-NMR (CDCl3, 300 MHz: δ 3.36 (s, 1H), 7.27 (dd, J=5 and 1 Hz, 2H), 7.40 (br s, 1H), 8.37 (d, J=8 Hz, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745477B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4d1fb41ff68347a19abf0fc18d688d1a
Quellennotizuspto-grants-2010_06