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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006936Generated: October 25, 2026

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

https://huagongshe.com/reaction/1006936

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 numberUS06790844B2
Source datasetuspto-grants-2004_09
ORD IDord-ad069d7b217e4c94a3e6947ba873653d
Source noteuspto-grants-2004_09