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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734818Generated: October 30, 2026

Triethylamine → HCID 18373051, compound

https://huagongshe.com/reaction/1734818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-DecyneHCID 12997—
Reactant5-Bromo-1-benzothiopheneHCID 2776578—
CatalystPalladium ChlorideHCID 24290—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18373051HCID 1837305189%

Reaction Steps

To a solution of 5-bromobenzothiophene (50.0 g), 1-decyne (35.7 g), triethylamine (71.2 g) and dry tetrahydrofuran (150 ml), under nitrogen, was added bis(triphenylphosphine)palladium (II) chloride (1.65 g) followed by copper (I) iodide (0.233 g) with stirring, at room temperature. The reaction mixture was covered with foil and stirred at reflux, under nitrogen, over the weekend. Additional bis-triphenylphosphine)palladium (II) chloride (0.5%) and 0.25% copper (I) iodide were added, and the reaction mixture was stirred at reflux for three days, cooled, filtered through a bed of celite and the filter cake was washed with ether. The residue was flash chromatographed (silica, 1% ethyl acetate-heptane). The appropriate fractions were collected and evaporated to give 56.3 g (89%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534636
Source datasetuspto-grants-1996_07
ORD IDord-9266216c042b4a36b5cb6b2f36bf47ad
Source noteuspto-grants-1996_07