Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403207Generated: November 2, 2026

Acetonitrile → [(4-Bromo-2-methoxyphenyl)ethynyl](trimethyl)silane

https://huagongshe.com/reaction/1403207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant4-Bromo-1-iodo-2-methoxybenzeneHCID 46835731—
CatalystHCID 178418476HCID 178418476—
Product[(4-Bromo-2-methoxyphenyl)ethynyl](trimethyl)silaneHCID 7123949696.5%

Reaction Steps

To a solution of 4-bromo-1-iodo-2-methoxybenzene (1.634 g, 5.221 mmol) in dry acetonitrile (20 mL) CuI (49.7 mg, 0.261 mmol) and Pd(Ph3P)2Cl2 (183.2 mg, 0.261 mmol) were added under Argon atmosphere and the mixture was degassed and backfilled with Argon for three times. TEA (0.728 mL, 5.221 mmol) and (ethynyl)trimethylsilane (1.48 mL, 1.03 g, 10.442 mmol) were added with a syringe and the reaction mixture, that darkened within 10 min, was stirred at room temperature for 1 h. The solvent was removed under vacuum and the residue was taken up with EtOAc (100 mL), washed with brine (3×20 mL), water (20 mL), dried over sodium sulphate and evaporated to dryness. The crude was purified by chromatography on silica gel (petroleum ether/diethyl ether 9/1) to yield the title compound as an orange solid (1.426 g, 96.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912200B2
Source datasetuspto-grants-2014_12
ORD IDord-8a9eb1b6ae634907ad4dd40e4180d91b
Source noteuspto-grants-2014_12