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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646266Generated: October 29, 2026

Hexane → HCID 59772707, compound

https://huagongshe.com/reaction/646266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTriethylamineHCID 8471—
Reactant4-iodo-1H-pyrrole-2-carbaldehydeHCID 4671953—
Reactant1-Bromo-3-ethynylbenzeneHCID 11480818—
CatalystCopper iodideHCID 83717—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59772707HCID 5977270793.5%

Reaction Steps

A solution of 4-iodo-1H-pyrrole-2-carbaldehyde (0.50 g; 2.262 mmol) and bis(triphenylphosphine)palladium-(II)chloride (0.079 g; 0.113 mmol)) in DMF (15 mL; degassed with nitrogen for 30 minutes) was stirred at ambient temperature for 15 minutes. Then the following were added: 1-bromo-3-ethynylbenzene (0.61 g; 3.394 mmol), copper iodide (43 mg; 0.226), and triethylamine (1.58 mL, 11.3 mmol). The course of the reaction was followed with TLC (4:1, hexane:ethyl acetate). After 2 hours the reaction mixture was diluted with water and the organic material was extracted into dichloromethane. The organic extracts were washed with water and brine, dried over MgSO4, filtered, and evaporated. The residue was chromatographed on silica gel using 3:1 hexane:ethyl acetate to yield 0.58 g (93%) of the title compound as a yellow crystalline solid, mp 152-156° C.; MS (ES) m/z 272.0, [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705030B2
Source datasetuspto-grants-2010_04
ORD IDord-a916635bf71d41eb9946a3191956a677
Source noteuspto-grants-2010_04