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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043005Generated: October 30, 2026

Trimethylsilylacetylene → HCID 58319144, compound

https://huagongshe.com/reaction/2043005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-(di-tert-butylphosphino)-N-phenylindoleHCID 11175133—
ReactantHCID 58319110HCID 58319110—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventN,N,N',N'-TetramethylethylenediamineHCID 8037—
ProductHCID 58319144HCID 58319144—

Reaction Steps

The title compound was prepared from and according to the general procedure A dry Schlenk flask was charged with methyl 2-(4-iodophenyl)cyclopropanecarboxylate (1.66 g, 5.49 mmol), Na2[PdCl4] (18 mg, 0.06 mmol), 2-(di-tert-butylphosphino)-1-phenylindole (37 mg, 0.11 mmol), CuI (21 mg, 0.11 mmol), and tetramethylethylenediamine (10 mL). The mixture was evacuated and backfilled with Ar (3×), and heated to 70° C. before addition of trimethylsilylacetylene (1.4 mL, 10.8 mmol) through the septum and the temperature was elevated to 80° C. After consumption of the starting material indicated by HPLC, the reaction mixture was cooled to room temperature, quenched with water and extracted with EtOAc (3×). The combined extracts were washed with brine, dried over MgSO4 and concentrated under vacuum and a fraction of the residue was purified by flash chromatography to give 580 mg (40%) after purification by flash chromatography (SiO2, EtOAc:PE, 1:8): Rt: 14.56 min (HPLC method I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586607B2
Source datasetuspto-grants-2013_11
ORD IDord-52fcee44589d4cdaba9ff40d1901e760
Source noteuspto-grants-2013_11