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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810712Generated: November 5, 2026

4-(2-Propyn-1-yl)morpholine → HCID 86629328, compound

https://huagongshe.com/reaction/1810712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Propyn-1-yl)morpholineHCID 412941—
ReactantHCID 86629329HCID 86629329—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 86629328HCID 86629328—

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Propargylmorpholine (0.64 g, 5.1 mmol) was added under nitrogen atmosphere to a degassed solution of ethyl (Z)-[7-[3-(4-iodophenyl)-3-(4-trifluoromethylphenyl)allyloxy]-benzo[b]furan-4-yl]oxyacetate (0.68 g, 1.09 mmol) in a mixture of tetrahydrofuran (20 mL) and triethylamine (10 mL) The solution was cooled to 0° C., tetrakis(triphenylphosphine)-palladium (0.17 g, 0.147 mmol) and copper(I) iodide (0.03 g, 0.16 mmol) were added. The reaction mixture was stirred at ambient temperature for 120 h, diluted with benzene (100 mL), decanted and evaporated in vacuo. The residue was purified by column chromatography (silica gel Fluka 60, benzene/ethyl acetate 1:0-0:1) yielding ethyl (E)-[7-[3-[4-[3-(morpholin-4-yl)propynyl]phenyl]-3-(4-trifluoromethylphenyl)allyloxy]benzo[b]furan-4-yl]oxyacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362016B2
Source datasetuspto-grants-2013_01
ORD IDord-60fb9a7734fc4f47846b5a636cf5affb
Source noteuspto-grants-2013_01