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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471396Generated: October 30, 2026

Triethylamine → 2-Methyl-5-((trimethylsilyl)ethynyl)pyridine

https://huagongshe.com/reaction/471396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Amino-5-bromopyridineHCID 70622—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Methyl-5-((trimethylsilyl)ethynyl)pyridineHCID 15553763—

Reaction Steps

The title compound is synthesized according to general procedure GP2 starting from 2.0 g (11.6 mmol) 5-bromo-pyridin-2-ylamine and 2.3 mL (16.3 mmol) 1-trimethylsilyl-ethyne using 68 mg (0.36 mmol) CuI, 305 mg (1.2 mmol) triphenylphosphine, 213 mg (0.30 mmol) PdCl2(PPh3)2 and 18 mL (127 mmol) triethylamine in 18 mL dry THF. For the work-up the reaction mixture is diluted with ethyl acetate, the organic phase is extracted with water and brine. The product is purified by chromatography on silica gel using a hexane/ethyl acetate gradient. Yield: 1.5 g (68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633183B2
Source datasetuspto-grants-2014_01
ORD IDord-c6709a8e8e55410ebd87ce266b9146e8
Source noteuspto-grants-2014_01