Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102915Generated: October 31, 2026

Cyclopropylacetylene → HCID 57804096, compound

https://huagongshe.com/reaction/2102915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylacetyleneHCID 138823—
ReactantMethyl 4-bromo-2-methylbenzoateHCID 22031226—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 57804096HCID 5780409671.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 4-Bromo-2-methylbenzoate (1.0 g, 4.4 mmol) was dissolved in triethylamine (5 mL). To the mixture was added copper iodide (43 mg, 5 mol %), followed by PdCl2(PPh3)2 (157 mg, 5 mol %) and ethynylcyclopropane (1.43 ml, 12 mmol). The mixture was heated in a sealed pressure tube at 80° C. for 3 hours. After completion of the reaction, the triethylamine was evaporated and the residue was dissolved in EtOAc and filtered through Celite®. The organic layer was washed with water, brine, and dried (Na2SO4), then filtered and concentrated under vacuum. The residue was purified by column chromatography on sililca gel using EtOAc-hexane (0-100% gradient) as eluent to give the desired product (630 mg). The product was dissolved in 10 mL of MeOH and 10 mL of 2N LiOH and the mixture was refluxed overnight. The MeOH was evaporated and the basic layer was washed with EtOAC, acidified, and re-extracted with EtOAC. The organic layer was washed with brine, dried (Na2SO4), filtered and concentrated under vacuum to give the desired product as a beige solid (461 mg). m/z 201 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576099B2
Source datasetuspto-grants-2009_08
ORD IDord-b5e27706ce004925b9df39ebb6fca80f
Source noteuspto-grants-2009_08