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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052308Generated: October 30, 2026

Dimethylformamide → [(2,6-Difluoro-3,5-dimethoxyphenyl)ethynyl](trimethyl)silane

https://huagongshe.com/reaction/1052308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2,4-Difluoro-3-iodo-1,5-dimethoxybenzeneHCID 86722805—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
Product[(2,6-Difluoro-3,5-dimethoxyphenyl)ethynyl](trimethyl)silaneHCID 8996336094.3%

Reaction Steps

To a stirred mixture of 2,4-difluoro-3-iodo-1,5-dimethoxybenzene (740 mg, 2.47 mmol), (trimethylsilyl)acetylene (0.697 mL, 4.93 mmol), copper(I) iodide (38 mg, 0.20 mmol), and triethylamine (0.52 mL, 3.7 mmol) in N,N-dimethylformamide (DMF) (4 mL, 50 mmol), bis(triphenylphosphine)palladium(II) chloride (86 mg, 0.12 mmol) was added. The reaction mixture was stirred at room temperature for 70 hours. The reaction was quenched with saturated aq. NH4Cl, then extracted with methylene chloride. The combined organic layers were dried over MgSO4, then concentrated. The residue was purified on silica gel (eluting with 0 to 30% EtOAc in hexanes) to give the desired product (630 mg, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388185B2
Source datasetuspto-grants-2016_07
ORD IDord-d2912e01a0ff4cc98eca9c1a70fdb86b
Source noteuspto-grants-2016_07