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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-chloro-2,5,6-trifluoropyridine | HCID 2783252 | — |
| Reactant | 3-Chloro-5-hydroxybenzonitrile | HCID 21949878 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Chloro-5-[(5-chloro-3,6-difluoropyridin-2-yl)oxy]benzonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404856B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-33da1d600aae494db34bd8cf32b5d5b2 |
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| Source note | uspto-grants-2013_03 |
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