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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515841Generated: October 30, 2026

Trimethylsilylacetylene → HCID 58368507, compound

https://huagongshe.com/reaction/515841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 58368557HCID 58368557—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 58368507HCID 5836850795.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of copper (I) iodide (1.1 g, 5.8 mmol) in triethylamine (32 mL) was degassed with nitrogen, treated with (trimethylsilyl)acetylene (4.5 mL, 32 mmol), degassed with nitrogen, and stirred at 20° C. for 10 minutes. The reaction mixture was treated with bis(triphenylphosphine)palladium(II) chloride (0.56 g, 0.80 mmol), degassed with nitrogen, and stirred at 20° C. for 30 minutes. The reaction mixture was treated with methyl 5-chloro-2-hydroxy-4-iodobenzoate (5.0 g, 16 mmol), degassed with nitrogen, and stirred at 75° C. for 2 hours. The reaction mixture was filtered over celite, washed with ethyl acetate, and concentrated to a crude residue. Purification via flash column chromatography using ethyl acetate in hexanes (0%-20%) gave the desired product (4.31 g, 95%). LCMS for C13H16ClO3Si (M+H)+: m/z=283.1; Found: 282.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108984B2
Source datasetuspto-grants-2015_08
ORD IDord-722b63a8166d479295464d17fada2f8a
Source noteuspto-grants-2015_08