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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847999Generated: November 4, 2026

Trimethylsilylacetylene → 2-Fluoro-4-((trimethylsilyl)ethynyl)aniline

https://huagongshe.com/reaction/1847999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiethyl EtherHCID 3283—
Product2-Fluoro-4-((trimethylsilyl)ethynyl)anilineHCID 22025680100.6%

Reaction Steps

A stirred mixture of 2-fluoro-4-iodoaniline (5.0 g, 21.1 mmol), CuI (90 mg, 0.42 mmol), and PdCl2(PPh3)2 (300 mg, 0.42 mmol) in a pressure tube was flushed with argon. Ethynyltrimethylsilane (2.28 g, 23.2 mmol) in TEA (20 mL) was added and the resulting mixture was stirred at rt over night. The reaction mixture was then diluted with Et2O and filtered through a Celite pad. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel chromatography eluting with 5% EtOAc in hexanes to afford 2-fluoro-4-((trimethylsilyl)ethynyl)aniline (4.4 g, 100%) as a brown solid. LCMS (ESI) m/z 208 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-0a581e6a72b24cae8a7d1b2b801d336b
Source noteuspto-grants-2015_02