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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432300Generated: November 1, 2026

Water → 2-Fluoro-6-(4-methylphenylthio)benzonitrile

https://huagongshe.com/reaction/432300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-MethylbenzenethiolHCID 7811—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-DifluorobenzonitrileHCID 74695—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Fluoro-6-(4-methylphenylthio)benzonitrileHCID 273740137%

Reaction Steps

A solution of 2,6-difluorobenzonitrile (5.18 g, 37.26 mmol) in dimethylformamide (100 mL) was treated with p-thiocresol (4.628 g, 37.26 mmol) and potassium carbonate (10.28 g, 74.52 mmol). The reaction mixture was stirred for 24 h under a nitrogen atmosphere. Water (150 mL) and ethyl acetate (250 mL) were added to the reaction mixture. The layers were partitioned and the aqueous layer was extracted with ethyl acetate (500 mL). The combined organic layers were washed with water (1 L), dried over magnesium sulfate, filtered and evaporated under reduced pressure. The crude product was purified by flash chromatography on silica gel, eluting 7:1 heptane:ethyl acetate. The column afforded 3.341 g (37%) of 2-fluoro-6-[(4-methylphenyl)sulfanyl]benzonitrile. 1H NMR (DMSO-d6, 400 MHz) δ 7.66-7.61 (m, 1H), 7.47-7.45 (m, 2H), 7.36-7.32 (m, 3H), 6.83-6.79 (m, 1H), 2.36 (s, 3H); HPLC Waters 2690 Alliance HPLC (Symmetry Shield RP18 3.5 μm, 2.1×50 mm; 5%-95% acetonitrile-0.1 M ammonium acetate over 15 min, 0.5 mL/min) Rt 8.04 min (93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660744B1
Source datasetuspto-grants-2003_12
ORD IDord-5bd12ea2126a43c595a5425eaf0e8831
Source noteuspto-grants-2003_12