Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598839Generated: October 29, 2026

Trimethylsilylacetylene → 6-((Trimethylsilyl)ethynyl)isoquinoline

https://huagongshe.com/reaction/598839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant6-BromoisoquinolineHCID 313681—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product6-((Trimethylsilyl)ethynyl)isoquinolineHCID 57950564101.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 6-bromoisoquinoline (2.0 g, 9.6 mmol) (commercially available from Gateway Chemical Technology, Inc.) in 45 mL of Et3N was added PdCl2(PPh3)2 (0.34 g, 0.48 mmol) and copper(I) iodide (0.27 g, 1.4 mmol). The mixture was degassed by bubbling nitrogen through the mixture for 1 minute. Ethynyltrimethylsilane (2.7 mL, 19 mmol) was added. The mixture was heated to 50° C. After 1 hour, the solvent was removed by rotary evaporation and the residue was purified by flash chromatography on silica gel (5% to 30% EtOAc/hexanes), affording 6-(2-(trimethylsilyl)ethynyl)isoquinoline (2.2 g, 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897619B2
Source datasetuspto-grants-2011_03
ORD IDord-6cc7540067a14f68abf611ed448f0765
Source noteuspto-grants-2011_03