HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348994Generated: October 26, 2026
Dimethylformamide → 2-Fluoro-6-(2-trifluoromethyl-4-thienyloxy)pyridine
https://huagongshe.com/reaction/1348994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Difluoropyridine | HCID 73934 | — |
| Reactant | 4-Hydroxy-2-(trifluoromethyl)thiophene | HCID 11084273 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Fluoro-6-(2-trifluoromethyl-4-thienyloxy)pyridine | HCID 12115991 | 74.3% |
Reaction Steps
1.00 g of 2,6-difluoropyridine is introduced into 10 ml of DMF under nitrogen and 1.44 g of K2CO3 are added at RT. 1.61 g of 4-hydroxy-2-trifluoromethylthiophene are added and the mixture is heated at 80° C. for 4 h, then cooled to RT and poured into water. After extraction twice with heptane/ethyl acetate (1:1) and twice with ethyl acetate the product is washed with water and saturated sodium chloride solution, dried over MgSO4 and concentrated. Chromatographic purification on silica gel with heptane/ethyl acetate (3:7) as eluent gives 1.7 g of 2-fluoro-6-(2-trifluoromethyl-4-thienyloxy)pyridine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211673B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-9169015d135343b7bf4f71314f831d37 |
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| Source note | uspto-grants-2007_05 |
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