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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760086Generated: October 31, 2026

Diisopropylamine → Ethyl 4-((trimethylsilyl)ethynyl)benzoate

https://huagongshe.com/reaction/1760086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl 4-bromobenzoateHCID 22043—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-((trimethylsilyl)ethynyl)benzoateHCID 1072913473%

Reaction Steps

A mixture of ethyl 4-bromobenzoate (1.5 g, 6.55 mmol), ethynyl trimethylsilane (965 mg, 9.82 mmol), diisopropylamine (1.39 g, 13.7 mmol), cuprous iodide(25 mg, 0.131 mmol), and bis(triphenylphosphine) palladium(II) chloride (184 mg, 0.262 mmol) was heated at 45° C. for 4 h in dry THF (10 ml) under argon atmosphere. The reaction was quenched by the addition of water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated. The residue was purified by silica gel flash column chromatography (eluent: hexane/ethyl acetate=100/1) to give ethyl 4-[(trimethylsilyl)ethynyl]benzoate (73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838574B1
Source datasetuspto-grants-2005_01
ORD IDord-a380b7e5e4f24eaeb9ef279e84ab3e9e
Source noteuspto-grants-2005_01