HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56855Generated: October 25, 2026
Potassium Hydroxide → 5-(Difluoromethoxy)-4-iodo-2-methoxypyridine
https://huagongshe.com/reaction/56855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Difluoromethyl trifluoromethanesulfonate | HCID 542802 | — |
| Reactant | 4-Iodo-6-methoxypyridin-3-ol | HCID 12027786 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(Difluoromethoxy)-4-iodo-2-methoxypyridine | HCID 117605317 | — |
Reaction Steps
4.8 ml of aqueous potassium hydroxide solution (6M) were added to a solution of 600 mg (purity 93%, 2.22 mmol) of 4-iodo-6-methoxypyridin-3-ol in 4.8 ml of acetonitrile, the mixture was cooled in an ice bath and 863 μl (purity 75%, 3.56 mmol, 1.6 eq.) of difluoromethyl trifluoromethanesulphonate [Angew. Chem. Int. Ed. 2013, 52, 1-5; Journal of Fluorine Chemistry 2009, 130, 667-670] were added with vigorous stirring. The reaction mixture was stirred for 2 min and diluted with 33 ml of water. The aqueous phase was extracted twice with in each case 40 ml of diethyl ether. The combined organic phases were dried (sodium sulphate), filtered, concentrated under reduced pressure and dried. The crude product was purified by flash chromatography (IR-50SI, petroleum ether/ethyl acetate 12-20%). Yield: 407 mg (purity 90%, 55% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434690B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-fcb6b0de660543c1a3e2b855c42f019b |
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| Source note | uspto-grants-2016_09 |
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