HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049578Generated: October 31, 2026
((1,1-Dimethyl-2-propynyl)oxy)trimethylsilane → HCID 131736032, compound
https://huagongshe.com/reaction/1049578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | ((1,1-Dimethyl-2-propynyl)oxy)trimethylsilane | HCID 87344 | — |
| Reactant | HCID 117759730 | HCID 117759730 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 131736032 | HCID 131736032 | — |
Reaction Steps
Under a nitrogen atmosphere, to a mixture of 4-((tert-butoxycarbonyl)oxy)-2′-fluoro-5′-methoxybiphenyl-2-yl trifluoromethanesulfonate (408 mg), tetrakis(triphenylphosphine)palladium (308 mg), copper iodide (32 mg) and triethylamine (10 mL) was added trimethyl((2-methylbut-3-yn-2-yl)oxy)silane (1.7 mL). The mixture was stirred at 80° C. for 15 hr, and tetrakis(triphenylphosphine)palladium (308 mg) was added. The mixture was stirred at 80° C. for 20 hr, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (232 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382188B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-b0c98111ffd843d081cf327cb53162ba |
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| Source note | uspto-grants-2016_07 |
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