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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456871Generated: October 29, 2026

Trimethylsilylacetylene → Methyl 2-chloro-5-((trimethylsilyl)ethynyl)benzoate

https://huagongshe.com/reaction/456871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantMethyl 2-chloro-5-iodobenzoateHCID 35563912—
CatalystTriphenylphosphineHCID 11776—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418903HCID 178418903—
SolventTriethylamineHCID 8471—
ProductMethyl 2-chloro-5-((trimethylsilyl)ethynyl)benzoateHCID 5742292998.1%

Reaction Steps

A mixture of 2-chloro-5-iodo-benzoic acid methyl ester (3.5 g, 12 mmol), dichlorobis(triphenylphosphino)palladium(II) (0.04 g, 0.06 mmol), triphenylphosphine (0.06 g, 0.24 mmol), copper iodide (0.05 g, 0.24 mmol), (trimethylsilyl)acetylene (1.9 g, 19.2 mmol) in triethylamine (40 mL) was heated at reflux for 12 h. The mixture was concentrated in vacuo, diluted with ethyl acetate (150 mL) and washed sequentially with 10% aqueous citric acid, water, and brine. The organic solution was dried, filtered and concentrated in vacuo to afford the title compound (3.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186742B2
Source datasetuspto-grants-2007_03
ORD IDord-35f1d8e447844d7bb99c7c89a2e4d1d5
Source noteuspto-grants-2007_03