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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071331Generated: November 3, 2026

Water → 4-[(trimethylsilyl)ethynyl]benzyl tert-butyldiphenylsilyl Ether

https://huagongshe.com/reaction/1071331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantSilane, [(4-bromophenyl)methoxy](1,1-dimethylethyl)diphenyl-HCID 14903624—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDiethyl EtherHCID 3283—
Product4-[(trimethylsilyl)ethynyl]benzyl tert-butyldiphenylsilyl EtherHCID 10297175—

Reaction Steps

A 25 mL round bottom flask was flame-dried under high vacuum. The vacuum was broken by the addition of dry argon, and the flask was allowed to cool to room temperature. The flask was charged with 2.0 g (4.70 mmol) of 4-bromobenzyl tert-butyldiphenylsilyl ether (Compound 1), 2.0 mL (14.1 mmol) of (trimethylsilyl)acetylene, and 16.5 mL of triethylamine. The solution was purged with argon for 15 minutes and bis(triphenylphosphine)palladium (II) chloride (83 mg, 0.12 mmol) and copper (I) iodide (22 mg, 0.12 mmol) were added and the solution stirred at ambient temperature for 3 days. The solution was poured into a separatory funnel containing water and ether. The layers were separated and the aqueous layer was extracted 3 times with ether. The combined ether layers were washed once with brine, and dried over magnesium sulfate, and the solvents were removed under reduced pressure. The residue was purified by distillation (bp=180° B 185° C., 1 torr) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906057B1
Source datasetuspto-grants-2005_06
ORD IDord-db1a1e831f5947948043a84a6843c17d
Source noteuspto-grants-2005_06