Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 1-fluoro-2-methyl-4-nitro- | HCID 68001 | — |
| Reactant | 2-Chloro-5-hydroxypyridine | HCID 819821 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86650898 | HCID 86650898 | — |
Reaction Steps
To a suspension of 6-chloropyridin-3-ol (3.37 g, 26.0 mmol) and K2CO3 (7.19 g, 52.0 mmol) in DMF (200 mL) was added 1-fluoro-2-methyl-4-nitrobenzene (4.44 g, 28.6 mmol). After heating to 50° C. for 16 hours, the reaction mixture was cooled to room temperature and poured into water and extracted with ethyl acetate (2×). The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to provide the product as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08648087B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7b8c3702e2ab4f8894c8f0536c0e97fa |
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| Source note | uspto-grants-2014_02 |
|---|