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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735004Generated: October 30, 2026

Piperidine → 1-(4-Trimethylsilanylethynylbenzyl)pyrrolidine

https://huagongshe.com/reaction/735004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant1-(4-Iodobenzyl)pyrrolidineHCID 18525867—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Product1-(4-Trimethylsilanylethynylbenzyl)pyrrolidineHCID 68816740—

Reaction Conditions

Temperature0 °C

Reaction Steps

A reaction mixture of 1 g (3.48 mmol) of 1-(4-iodobenzyl)pyrrolidine, 5 mL of piperidine, 105 mg (0.091 mmol) of tetrakistriphenylphosphine palladium, and 10 mg (0.053 mmol) of copper (I) iodide is cooled to 0° C. At this temperature, 0.59 mL (4.18 mmol) of trimethylsilylacetylene is added dropwise and then the cooling bath is removed. It is stirred for 3 hours at ambient temperature, then combined with a saturated aqueous ammonium chloride solution, and extracted with dichloromethane. The organic phase is dried over sodium sulfate. The purification is carried out by column chromatography on silica gel (eluant: cyclohexane/ethyl acetate (1:1)). Yield: 0.75 g (83.6% of theory); C16H23NSi (M=257.45); calc.: molecular ion peak (M+H)+: 258; found: molecular ion peak (M+H)+: 258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592373B2
Source datasetuspto-grants-2009_09
ORD IDord-ce67a05fc9e848069826b7a802e34465
Source noteuspto-grants-2009_09