Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974160Generated: October 26, 2026

Trimethylsilylacetylene → 1-(5Methylpyridin-2-yl)-2-(2,3-difluoro-4-ethoxyphenyl) acetylene

https://huagongshe.com/reaction/974160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Bromo-5-methylpyridineHCID 564216—
Reactant2-Ethynyl-5-methylpyridineHCID 13400634—
Reactant1-Ethoxy-2,3-difluoro-4-iodobenzeneHCID 22008078—
CatalystPalladiumHCID 23938—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTriethylamineHCID 8471—
Product1-(5Methylpyridin-2-yl)-2-(2,3-difluoro-4-ethoxyphenyl) acetyleneHCID 17978010—

Reaction Steps

A mixture of 0.01 mol of 5-methylpyridin-2-yl-acetylene (which can be prepared from 5-methyl-2-bromopyridine by reaction with trimethylsilyl-acetylene and Pd catalyst and subsequent splitting off of the trimethylsilyl group), 0.01 mol of 4-iodo-2,3-difluorophenetole (for the preparation, see Example 9), 30 ml of triethylamine, 0.2 mmol of Pd catalyst and 0.1 mmol of CuI is stirred at room temperature for 24 hours. The reaction mixture is diluted with petroleum ether and filtered over silica gel. Evaporation and purification give 1-(5methylpyridin-2-yl)-2-(2,3-difluoro-4-ethoxyphenyl) acetylene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068053
Source datasetuspto-grants-1991_11
ORD IDord-e5c2e1a1e50d4ddf8f8539b7d732b4a3
Source noteuspto-grants-1991_11