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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 491034Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/491034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-IodoanilineHCID 11995—
Edukt(But-3-yn-1-yloxy)(tert-butyl)dimethylsilaneHCID 4304567—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTriethylamineHCID 8471—
Produkt2-[4-(tert-Butyldimethylsilanyloxy)but-1-ynyl]phenylamineHCID 57675740—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07528262B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-3c47387b6f994676a8996f74a6e2aa36
Quellennotizuspto-grants-2009_05