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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157173Generated: November 2, 2026

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

https://huagongshe.com/reaction/1157173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIodobenzeneHCID 11575—
Reactanttert-Butyl 4-ethynylpiperidine-1-carboxylateHCID 15550481—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
ProductN-BOC-4-(phenylethynyl)piperidineHCID 1798699325.9%

Reaction Steps

Iodobenzene (135 μl, 1.2 mmols), 4-ethynyl-piperidine-1-carboxylic acid tert-butyl ester (209 mg, 1 mmols) and triethylamine (167 μl, 1.2 mmols) were dissolved in acetonitrile (6 ml). Dichlorobis(triphenylphosphine)palladium(II) (35 mg, 0.05 mmols) and Cul (10 mg, 0.05 mmols) were added, and reaction mixture was stirred at room temperature overnight and continued to stir at 50 C. for two more hours before partitioning between ethyl acetate and water. Organic layer was isolated, washed with 1 N HCl, brine and dried (MgSO4). Solvents were removed and residue was purified by column chromatography on silica gel using solutions of ethyl acetate in hexanes (1:4; 1:2) to yield the title compound (74 mg). LCMS m/e (230, M−t-Bu+2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807672B2
Source datasetuspto-grants-2010_10
ORD IDord-fcb2bd50885246cd8226fd60faee832b
Source noteuspto-grants-2010_10