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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936222Generated: November 2, 2026

Trimethylsilylacetylene → HCID 67484047, compound

https://huagongshe.com/reaction/1936222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3-Cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl esterHCID 67483447—
CatalystTriethylamineHCID 8471—
CatalystIodide IonHCID 30165—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDimethylformamideHCID 6228—
ProductHCID 67484047HCID 6748404793.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-cyclopentyl-2-(4-iodo-phenyl)-propionic acid methyl ester (716 mg, 2.0 mmol) and triethylamine (2 mL, 0.01 mmol) in N,N-dimethylformamide (2 mL) was treated with trimethylsilyl acetylene (0.71 mL, 5.0 mmol). The resulting reaction mixture was degassed with argon and then treated with cooper iodide (10 mg, 0.05 mmol) and bis(triphenylphosphine)palladium (II) chloride (15 mg, 0.02 mmol). The reaction was then heated at 70° C. for 24 h. At this time, the reaction was cooled to 25° C. and concentrated in vacuo. The residue was diluted with ethyl acetate (40 mL) and washed with a half-saturated aqueous sodium chloride solution (1×20 mL). The resulting aqueous layer was back extracted with ethyl acetate (1×40 mL). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 60/40 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-trimethylsilanylethynyl-phenyl)-propionic acid methyl ester (615 mg, 93.6%) as an orange solid: mp 72-74° C.; EI-HRMS m/e calcd for C20H28O2Si (M+) 328.1858, found 328.1852.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388071B2
Source datasetuspto-grants-2002_05
ORD IDord-9a780aeec1a04ecdaf62b79da8ce0e15
Source noteuspto-grants-2002_05