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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074314Generated: November 2, 2026

Iodobenzene → N-BOC-4-(phenylethynyl)piperidine

https://huagongshe.com/reaction/2074314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodobenzeneHCID 11575—
Reactanttert-Butyl 4-ethynylpiperidine-1-carboxylateHCID 15550481—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
ProductN-BOC-4-(phenylethynyl)piperidineHCID 1798699390.9%

Reaction Steps

Tert-butyl 4-ethynylpiperidine-1-carboxylate (12.5 g) and iodobenzene (12.8 g) was dissolved in THF:TEA=1:1 (v/v) mixed solvent (125 ml), then at room temperature, copper iodide (455 mg) and palladium tetrakistriphenylphosphine complex (1.38 g) were added thereto in that order, followed by stirring overnight at room temperature. The solvent was evaporated, EtOAc was added to it, and washed with aqueous 1 M hydrochloric acid solution, water and saturated brine in that order. This was dried over magnesium sulfate, and the solvent was evaporated to obtain a light brown oil. This was purified by silica gel column chromatography (eluent: hexane:EtOAc=19:1 (v/v)) to obtain tert-butyl 4-(phenylethynyl)piperidine-1-carboxylate (15.5 g) as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919495B2
Source datasetuspto-grants-2011_04
ORD IDord-1667f80477fa4cb380236c04e925799a
Source noteuspto-grants-2011_04