HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505965Generated: November 3, 2026
Trimethylsilylacetylene → 5-[(Trimethylsilyl)ethynyl]pyrimidine
https://huagongshe.com/reaction/505965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 5-Bromopyrimidine | HCID 78344 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diisopropylamine | HCID 7912 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-[(Trimethylsilyl)ethynyl]pyrimidine | HCID 15349669 | 85% |
Reaction Steps
Tetrakis(triphenylphosphine)palladium(O) (727 mg, 0.6 mmol) was added to a stirred, degassed suspension of 5-bromopyrimidine (5.0 g, 31.4 mmol) and copper(I)iodide (120 mg, 0.6 mmol) in toluene and diisopropylamine (1:1, 200 ml) under nitrogen. The reaction mixture was heated to 60° C., trimethylsilylacetylene (4.89 ml, 34.6 mmol) was added and the reaction mixture was stirred for 3 hours at 60° C. The reaction mixture was allowed to cool to room temperature, diluted with ethyl acetate (200 ml) and washed with saturated aqueous ammonium chloride solution (3×100 ml). The organic layer was separated, dried over MgSO4 and concentrated in vacuo. The crude product was purified by flash column chromatography (5% ethyl acetate/heptane) to give 5-trimethylsilanylethynyl-pyrimidine as a pale brown solid, 4.71 g (85% yield). LC at 215 nm; Rt 2.07: 88%, m/z (ES+): 177 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781593B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-ed51dcd02f0d49728475eac21d451aa2 |
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| Source note | uspto-grants-2010_08 |
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