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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977553Generated: October 27, 2026

Triethylamine → 2-(1-Dodecynyl)thiophene

https://huagongshe.com/reaction/977553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-IodothiopheneHCID 18921—
Reactant1-DodecyneHCID 69821—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Dodecynyl)thiopheneHCID 18372993739%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of 2-iodothiophene (31.5 g), 1-dodecyne (2.5 g), triethylamine (105 ml), and tetrahydrofuran (100 ml) was added (bis)triphenylphosphine palladium(II)chloride (1.73 g) followed by copper(I)iodide (0.24 g). The reaction mixture was warmed to 55° C. and stirred for 7 hr. The solution was allowed to cool to room temperature and stirred overnight. The mixture was filtered, and the precipitate was washed with ethyl acetate. The filtrate was diluted with ethyl acetate and washed with water and brine. The organic phase was separated, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was flash chromatographed over silica gel (eluted with hexane). The appropriate fractions were collected and evaporated. The residue was distilled to afford 27.6 g (74%) of product, bp 145°-150° C. at 0.7 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614631
Source datasetuspto-grants-1997_03
ORD IDord-ec30434d8b56461c85dad8e70fadb2c6
Source noteuspto-grants-1997_03