HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958754Generated: October 31, 2026
Triethylamine → 2-Methoxy-5-((trimethylsilyl)ethynyl)pyrimidine
https://huagongshe.com/reaction/1958754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyltrimethylsilane | HCID 137936 | — |
| Reactant | Pyrimidine, 5-bromo-2-methoxy- | HCID 139657 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Methoxy-5-((trimethylsilyl)ethynyl)pyrimidine | HCID 68742272 | 98.2% |
Reaction Steps
To a solution of 5-bromo-2-methoxypyrimidine (500 mg, 2.7 mmol) in ethyl acetate (2 mL) and water (0.2 mL) was added trimethylsilylethane (0.41 mL, 3 mmol), triethylamine (0.75 mL, 5.4 mmol), copper iodide (25 mg, 0.13 mmol) and bis(triphenylphosphine)palladium(II) dichloride (47 mg, 0.067 mmol). The solution was heated to 60° C. for 16 h. Ethyl acetate (100 mL) was added and the solution was washed with water (3×10 mL), dried over MgSO4 and treated with decolorizing charcoal. Ethyl acetate was removed in vacuo to give the title compound as a clear oil (547 mg, 97%). 1H NMR (400 MHz, CDCl3) δ 8.56 (s, 2H), 4.01 (s, 3H), 0.24 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410150B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-d12bb0f6e77d481898d35bb13a2dc50d |
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| Source note | uspto-grants-2013_04 |
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