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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665995Generated: October 26, 2026

Potassium Carbonate → 2-(4-Amino-3-methylphenoxy)-5-fluorobenzonitrile

https://huagongshe.com/reaction/1665995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Amino-m-cresolHCID 17819—
Reactant2,5-DifluorobenzonitrileHCID 123558—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-(4-Amino-3-methylphenoxy)-5-fluorobenzonitrileHCID 5741875599%

Reaction Steps

In a 3 L, 4-necked flask that had been evacuated and back-filled with argon, 2,5-difluorobenzonitrile (295.3 ml, 812.0 mmol) and 4-amino-3-methylphenol (100.0 g, 812.0 mmol) were dissolved in dry DMSO (2.75 M) with rapid stirring at room temperature. The solution was evacuated/backfilled with argon (3×). Potassium carbonate (185.2 g, 1340 mmol) (−325 mesh) was added. The reaction mixture was evacuated/backfilled with argon (3×) and warmed to 80° C. (internal probe) for 16 hours. TLC indicated complete conversion. The reaction mixture was cooled to room temperature and poured slowly into 2 L of ice water with rapid stirring. The residue in the round bottom flask was taken up in water repeatedly and poured into the ice water until a total volume of 3 L was achieved and all solids were in the ice water. The suspension was stirred rapidly for 2 hours as it came to room temperature. The brown solids were collected by filtration, washed with water (3 L), air dried, dried with latex dam, and dried under high vacuum at 40° C. for 44 hours to provide 194 g (99%) of the desired product as a tan solid. MS (APCI+) m/z 243 (M+1) was detected. 1H NMR (400 MHz, CDCl3) δ 7.38 (m, 1H), 7.18 (m, 1H), 6.65-6.85 (m, 5H), 3.60 (br, 2H), 2.17 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039639B2
Source datasetuspto-grants-2011_10
ORD IDord-31bd66f5995441bca818751981f0354c
Source noteuspto-grants-2011_10