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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690964Generated: October 26, 2026

Ammonium Chloride → (3-(4-Benzyloxy-phenyl)-prop-1-ynyl)-trimethylsilane

https://huagongshe.com/reaction/1690964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant4-Benzyloxybenzyl chlorideHCID 70042—
ReactantHCID 178418443HCID 178418443—
Catalystcopper(I) bromideHCID 24593—
SolventTetrahydrofuranHCID 8028—
Product(3-(4-Benzyloxy-phenyl)-prop-1-ynyl)-trimethylsilaneHCID 4264273172%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of trimethylsilyl acetylene (851 μL, 6.02 mmol) in tetrahydrofuran (20 mL) was added ethyl magnesium bromide (3 M diethyl ether solution, 1.86 mL, 5.59 mmol) under nitrogen atmosphere at room temperature, which was stirred for 40 minutes at 65° C. The reaction solution was cooled to room temperature, and copper (I) bromide (308 mg, 2.16 mmol) and 4-benzyloxybenzyl chloride (1.00 g, 4.30 mmol) were added to the reaction solution and stirred for 8 hours and 45 minutes at 65° C. Saturated ammonium chloride solution was added to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=30:1) to obtain the title compound (911 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-95e54dfce83d4463a9ac2137548f9520
Source noteuspto-grants-2012_04