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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363250Generated: October 26, 2026

Nitrogen → 4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1363250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPhenylacetyleneHCID 10821—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
CatalystCopper iodideHCID 83717—
CatalystBis(benzonitrile)palladium chlorideHCID 498840—
SolventDiisopropylamineHCID 7912—
Product4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehydeHCID 273713988.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

Under a N2 atmosphere, 4-bromothiophene-2-carbaldehyde (1.0 g, 5.2 mmol) was taken up in diisopropylamine (20 mL). TPP (549 mg, 2.1 mmol), bis(benzonitrile)palladium chloride ([Pd(PhCN)2]Cl2) (400 mg, 1.0 mmol), and copper iodide (199 mg, 1.0 mmol) were added. The mixture was degassed with N2 before phenylacetylene (1.15 mL, 10.4 mmol) was added, and the reaction was stirred at 70° C. for 16 h. The mixture was concentrated to a dark brown solid and chromatographed in 0-15% EtOAc in heptane to yield 4-(phenylethynyl)thiophene-2-carbaldehyde (981 mg, 88%). 1H NMR (400 MHz, CDCl3) δ (ppm): 9.93 (d, 1H), 7.88 (t, 1H), 7.85 (d, 1H), 7.53 (m, 2H), 7.38 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884124B2
Source datasetuspto-grants-2011_02
ORD IDord-0c28c548d6ce41eab751f5073a9f5344
Source noteuspto-grants-2011_02