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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19783Generated: October 25, 2026

Ammonium Chloride → 2-Chloro-4-ethynylpyridine

https://huagongshe.com/reaction/19783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-Chloro-4-(2-(trimethylsilyl)ethynyl)pyridineHCID 21985391—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-4-ethynylpyridineHCID 2343683191.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745477B2
Source datasetuspto-grants-2010_06
ORD IDord-4d1fb41ff68347a19abf0fc18d688d1a
Source noteuspto-grants-2010_06