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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735307Generated: October 30, 2026

Ethylene Glycol → 2-{[6-(2,4-Difluorophenyl)-2-naphthyl]thio}benzonitrile

https://huagongshe.com/reaction/735307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium CarbonateHCID 11430—
Reactant2-IodobenzonitrileHCID 2759358—
Reactant6-(2,4-Difluorophenyl)-2-naphthyl hydrosulfideHCID 68901488—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product2-{[6-(2,4-Difluorophenyl)-2-naphthyl]thio}benzonitrileHCID 6889915720.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

6-(2,4-Difluorophenyl)-2-naphthyl hydrosulfide (Step 2, 0.78 g) was dissolved in isopropyl alcohol (15 mL). 2-Iodobenzonitrile (0.66 g, 2.88 mmol), copper(I) iodide (29 mg, 0.15 mmol), potassium carbonate (0.8 g, 5.79 mmol) and ethylene glycol (320 μL) were added and the reaction heated to 80° C. under nitrogen overnight. Ethyl acetate was added to the cooled reaction mixture and stirred for 15 minutes. The mixture was filtered and the filtrate evaporated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 10-20% ethyl acetate/isohexane, followed by recrystallisation from ethyl acetate/isohexane, to give 2-{[6-(2,4-difluorophenyl)-2-naphthyl]thio}benzonitrile (216 mg, 20%). 1H NMR (500 MHz, CDCl3) δ 8.04 (1H, s), 7.97 (1H, s), 7.88 (2H, t, J=7.8 Hz), 7.68 (2H, d, J=8.0 Hz), 7.54-7.48 (2H, m), 7.43-7.39 (1H, m), 7.28 (1H, t, J=7.6 Hz), 7.19 (1H, d, J=7.9 Hz), 7.03-6.95 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592456B2
Source datasetuspto-grants-2009_09
ORD IDord-f6438c4c933b4f62ab5370b0a7332d8c
Source noteuspto-grants-2009_09