Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952336Generated: November 3, 2026

Water → 3-Chloro-5-[(5-chloro-3,6-difluoropyridin-2-yl)oxy]benzonitrile

https://huagongshe.com/reaction/1952336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-chloro-2,5,6-trifluoropyridineHCID 2783252—
Reactant3-Chloro-5-hydroxybenzonitrileHCID 21949878—
SolventDimethylformamideHCID 6228—
Product3-Chloro-5-[(5-chloro-3,6-difluoropyridin-2-yl)oxy]benzonitrileHCID 59529760—

Reaction Steps

A solution of 3-chloro-5-cyanophenol (1-4; 218 mg; 1.41 mmol) and 3-chloro-2,5,6-trifluoropyridine (1-5; 250 mg; 1.49 mmol) in anhydrous DMF (2 mL) was cooled to −40° C. under a nitrogen atmosphere. The reaction mixture was then treated with 260 mg (1.94 mmol) of anhydrous potassium carbonate added in one portion, and the reaction mixture was vigorously stirred and allowed to warm to room temperature slowly over 90 minutes. The reaction mixture was then stirred for another hour at room temperature. The reaction mixture was diluted with a large excess of water, and a thick precipitate formed. After trituration, the suspension was filtered and the solid dried to give the title compound as an off white amorphous solid. 1H NMR (CDCl3): 7.91 (m, 2H), 7.99 (t, 1H), 8.60 (q, 1H). MS M+1=302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404856B2
Source datasetuspto-grants-2013_03
ORD IDord-33da1d600aae494db34bd8cf32b5d5b2
Source noteuspto-grants-2013_03