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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814492Generated: October 25, 2026

4-Bromothiophene-3-carboxaldehyde → HCID 22503031, compound

https://huagongshe.com/reaction/1814492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromothiophene-3-carboxaldehydeHCID 2764207—
Reactant1-Ethynyl-4-(methoxymethoxy)benzeneHCID 22502995—
CatalystTriethylamineHCID 8471—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 22503031HCID 2250303166.9%

Reaction Steps

3-Formyl-4-bromothiophene (14.7 g) was dissolved in DMF (100 ml), followed by the addition of triethylamine (100 ml) CuI (0.25 g), Pd(PPh3)2Cl2 (0.5 g) and 4-methoxymethoxy-1-ethynylbenzene (11.4 g), and the mixture was reacted at 70° C. overnight. The reaction solution was filtered through Celite, poured into 1N hydrochloric acid, and then extracted with ethyl acetate. The organic layer was washed with an aqueous solution of saturated sodium bicarbonate and brine, dried and evaporated. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate system), to give 3-{[4-(methoxymethoxy)phenyl]ethynyl}-4-formylthiophene as a colorless oil (12.8 g, yield; 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-0246105bfa19470789925f21a1f1695b
Source noteuspto-grants-2005_04