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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519697Generated: November 5, 2026

Trimethylsilylacetylene → N-(1-{4-[(trimethylsilyl)ethynyl]phenyl}ethyl)cyclopropylamine

https://huagongshe.com/reaction/1519697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantN-[1-(4-iodophenyl)ethyl]cyclopropanamineHCID 43754631—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventChloroformHCID 6212—
ProductN-(1-{4-[(trimethylsilyl)ethynyl]phenyl}ethyl)cyclopropylamineHCID 7126817467.9%

Reaction Steps

Ethynyl(trimethyl)silane (80 mg), PdCl2(PPh3)2 (29 mg), CuI (16 mg), and TEA (0.25 g) were added to a chloroform (5.0 mL) solution of N-[1-(4-iodophenyl)ethyl]cyclopropylamine (0.23 g) as obtained in Example 14-(1), and the mixture was stirred in a nitrogen atmosphere for 24 hours at room temperature. Further, stirring was continued for 2 hours at 45° C., and then PdCl2(PPh3)2 (29 mg) was added. After the system was refluxed in a nitrogen atmosphere for 5 hours, the reaction mixture was concentrated. The resulting residue was purified by OH type silica gel chromatography (hexane/ethyl acetate=85/15) to obtain N-(1-{4-[(trimethylsilyl)ethynyl]phenyl}ethyl)cyclopropylamine (brown oil) (0.14 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-1696dfc1fb904c238ce7b179c9498e8e
Source noteuspto-grants-2015_07