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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264698Generated: October 26, 2026

2-Iodoaniline → 2-[4-(tert-Butyldimethylsilanyloxy)but-1-ynyl]phenylamine

https://huagongshe.com/reaction/2264698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodoanilineHCID 11995—
Reactant(But-3-yn-1-yloxy)(tert-butyl)dimethylsilaneHCID 4304567—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2-[4-(tert-Butyldimethylsilanyloxy)but-1-ynyl]phenylamineHCID 57675740—

Reaction Steps

2-Iodoaniline (1.76 g, 8 mmol) was dissolved in triethylamine (50 mL) and placed under N2. tert-Butylbut-3-ynyloxydimethylsilane (2.58 g, 14 mmol) was added, followed by bis(triphenylphosphine)palladium(II) chloride (30 mg, 0.042 mmol) and copper(I) iodide (7 mg, 0.036 mmol), and the reaction was stirred overnight at room temperature. Triethylamine was evaporated, and the residue was diluted with ether and filtered through Celite. The filtrate was concentrated, and the residue was purified by SiO2 chromatography (5-20% ethyl acetate/hexanes) to give the desired product. The reaction was assumed to be quantitative.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855224B2
Source datasetuspto-grants-2010_12
ORD IDord-2cbee858c1c5450d8ef1b2159c6a4acc
Source noteuspto-grants-2010_12