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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734779Generated: October 26, 2026

Tetrabutylammonium Fluoride → 5-(4-Chloro-phenyl)-2-ethynyl-pyridine

https://huagongshe.com/reaction/734779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-[(Tert-butyldimethylsilanyl)ethynyl]-5-(4-chlorophenyl)pyridineHCID 69058350—
SolventDichloromethaneHCID 6344—
Product5-(4-Chloro-phenyl)-2-ethynyl-pyridineHCID 57845328—

Reaction Steps

43.66 g (156.0 mmol) of TBAF was added to a solution of 46.50 g (142.0 mmol) of 2-[(tert-butyldimethylsilanyl)ethynyl]-5-(4-chlorophenyl)pyridine in 1 L of DCM at RT and the mixture was stirred for 2 hours. The organic phase was washed with water, dried over sodium sulfate, and evaporated down in vacuo. The residue was stirred with DIPE, and the precipitate was filtered off and washed with PE. Yield: 26.0 g (86% of theoretical); C13H8ClN (M=213.662); calc.: molpeak (M+H)+: 214/216 (Cl); found: molpeak (M+H)+: 214/216 (Cl); Rf value: 0.30 (silica gel, cyc/EtOAc 4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592358B2
Source datasetuspto-grants-2009_09
ORD IDord-c49bc3c416844058858140a2cd67f8ac
Source noteuspto-grants-2009_09