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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant((1,1-Dimethyl-2-propynyl)oxy)trimethylsilaneHCID 87344—
ReactantHCID 117759730HCID 117759730—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418397HCID 178418397—
SolventTriethylamineHCID 8471—
ProductHCID 131736032HCID 131736032—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-b0c98111ffd843d081cf327cb53162ba
Source noteuspto-grants-2016_07