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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301463Generated: October 30, 2026

Triethylamine → 2-(1-Dodecynyl)-4-thiophenecarboxaldehyde

https://huagongshe.com/reaction/2301463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-DodecyneHCID 69821—
Reactant5-Bromothiophene-3-carbaldehydeHCID 12284894—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Dodecynyl)-4-thiophenecarboxaldehydeHCID 18372976—

Reaction Steps

A solution of 2-bromo-4-thiophenecarboxaldehyde (45.3 g), 1-dodecyne (43.4 g), and triethylamine (99 ml), in dry tetrahydrofuran (250 ml) was chilled to 5° C. and degassed under nitrogen. bis(Triphenylphosphine)palladium(II)chloride (1.66 g) and copper(I)iodide (0.23 g) were added to the reaction mixture. The mixture was degassed and stirred overnight, under nitrogen, as it was allowed to warm to room temperature. The precipitate was filtered off, washed with ethyl acetate, and the filtrate was evaporated. Ethyl acetate was added to the residue. The solution was washed with brine, dried over magnesium sulfate, filtered, and the filtrate was concentrated. The residue was chromatographed through a silica gel pad eluting with heptane/1% ethyl acetate. The appropriate fractions were collected and evaporated. The residue and that from a similar reaction on a 0.05 mole scale were combined and distilled to give 30.7 g (79.5%), bp 181-185° C. @ 0.35 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500849B1
Source datasetuspto-grants-2002_12
ORD IDord-6c6428ce19e94fafbf6c09c7aacc4972
Source noteuspto-grants-2002_12