Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243160Generated: November 2, 2026

Water → HCID 86593496, compound

https://huagongshe.com/reaction/2243160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Iodo-4-(trifluoromethoxy)benzeneHCID 2777294—
Reactant5-(4-trifluoromethoxy-phenyl)-1H-indoleHCID 10286124—
Catalystcopper(I) bromideHCID 24593—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86593496HCID 8659349644.4%

Reaction Steps

A mixture of 0.6 g (2.6 mmol) 5-(4-trifluoromethoxy-phenyl)-1H-indole, 0.53 mL (2.8 mmol) 4-(trifluoromethoxy)iodobenzene, 0.075 g (0.52 mmol) copper(I) bromide and 0.54 g (3.9 mmol) K2CO3 in 10 mL anhydrous N-methyl pyrrolidinone was heated to reflux overnight with stirring. The reaction was allowed to cool and was then poured into 200 mL of water. The aqueous solution was shaken with 200 mL ethyl acetate, the combined aqueous and organic phases were filtered, and the organic phase was separated. The aqueous phase was extracted once more with 200 mL ethyl acetate and the combined organic phases were washed with brine and concentrated. The crude product was chromatographed on silica (5-7% EtOAc-hexane as elutant) to afford 0.505 g (44% yield) of 1,5-bis-(4-trifluoromethoxy-phenyl)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674818B2
Source datasetuspto-grants-2010_03
ORD IDord-fe62d53ba2b04a6685a06a31259cceb8
Source noteuspto-grants-2010_03