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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535692Generated: October 29, 2026

Potassium Carbonate → HCID 71080370, compound

https://huagongshe.com/reaction/535692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantBenzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
CatalystCupric acetateHCID 8895—
Catalystcopper(I) bromideHCID 24593—
SolventDimethylformamideHCID 6228—
ProductHCID 71080370HCID 7108037023.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-Iodo-4-(trifluoromethyl)benzene (1.657 g, 6.09 mmol) was added to a solution of 5-bromo-1H-pyrrolo[2,3-b]pyridine (1 g, 5.08 mmol) and Copper(I) bromide (0.073 g, 0.508 mmol) in DMF (10 mL) followed by potassium carbonate (1.75 g, 12.69 mmol), and the mixture was stirred at 100° C. for 10 min. NaOH (150 mg, 3.75 mmol) and copper(II) acetate (4.61 mg, 0.025 mmol) were added to the reaction mixture at 110° C., and the mixture was stirred for 16 h. Insoluble solids were filtered off, and the filtrate was concentrated. Residue was partitioned between ethyl acetate and water. Organic layer was separated, washed with brine, dried over sodium sulphate, filtered and concentrated in vacuo. The crude product was purified by flash chromatography using 10% ethyl acetate in pet ether to afford title compound (0.4 g, 22%) as a off-white solid. 1H NMR (400 MHz, CDCl3): δ 8.4 (d, J=2.0 Hz, 1H), 8.11 (d, J=2.4 Hz, 1H), 7.93 (d, J=8.0 Hz, 2H), 7.78 (d, J=8.8 Hz, 2H), 7.56 (d, J=4.0 Hz, 1H), 6.63 (d, J=3.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859536B2
Source datasetuspto-grants-2014_10
ORD IDord-16ab87b1433a49589ec94160691a240a
Source noteuspto-grants-2014_10