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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856954Generated: October 31, 2026

Potassium Carbonate → HCID 21864973, compound

https://huagongshe.com/reaction/856954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,2',4'-TrichloroacetophenoneHCID 20250—
Reactant3-Hydroxynaphthalene-2-carbonitrileHCID 12990264—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 21864973HCID 2186497357.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 3-hydroxy-naphthalene-2-carbonitrile from step 2 (200 mg, 1.18 mmol) and 2,2′,4′-trichloroacetophenone (317 mg, 1.42 mmol, 1.2 eq) in anhydrous N,N-dimethylformamide (4.7 mL) was added potassium carbonate (326.7 mg, 2.36 mmol, 2.0 eq), and the orange reaction mixture was stirred at 80° C. for 16 h. The resulting dark wine colored reaction was diluted with ethyl acetate and water. The organic layer was washed with saturated aqueous ammonium chloride, water, brine, and dried over magnesium sulfate. The solvent was removed at reduced pressure and the crude product was purified on the MPLC (biotage) eluted with 15% ethyl acetate-hexane. Crystallization from ether-hexane afforded 243 mg (57.7%) of the desired benzofuran. 1H-NMR (DMSO-d6) δ 8.66 (s, 1H), 7.99 (d, J=8.1 Hz, 1H), 7.93 (d, J=8.1 Hz, 1H), 7.88 (s, 1H), 7.76 (d, J=1.5 Hz, 1H), 7.72 (broad s, 2H), 7.63 to 7.42 (m, 4H); LC-MS (ES MH+=356).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144885B2
Source datasetuspto-grants-2006_12
ORD IDord-51767a93a7d6407a989ec9f10d456abe
Source noteuspto-grants-2006_12