Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Bromo-1,3-difluoro-2-nitrobenzene | HCID 21335487 | — |
| Product | 5-Bromo-3-fluoro-2-nitroanisole | HCID 57955648 | 63% |
Reaction Steps
To a solution of 5-bromo-1,3-difluoro-2-nitrobenzene (2.7 g, 11.3 mmol) in methanol (20 mL) was added potassium hydroxide (680 mg, 12 mmol). The reaction mixture was refluxed at 90° C. for 1 h. It was then concentrated, diluted to ethyl acetate and washed by water and brine. The mixture was then purified by flash column to give the product as red oil (1.8 g, 63%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 3.94 (s, 3 H) 7.01 (s, 1 H) 7.04 (d, J=8 Hz, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318727B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-4ecd0678cc8e456bba1e06c721706bf6 |
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| Source note | uspto-grants-2012_11 |
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