HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043005Generated: October 30, 2026
Trimethylsilylacetylene → HCID 58319144, compound
https://huagongshe.com/reaction/2043005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 2-(di-tert-butylphosphino)-N-phenylindole | HCID 11175133 | — |
| Reactant | HCID 58319110 | HCID 58319110 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Product | HCID 58319144 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586607B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-52fcee44589d4cdaba9ff40d1901e760 |
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| Source note | uspto-grants-2013_11 |
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