HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 2-fluoro-5-methoxy-4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Methyl 2,5-difluoro-4-nitrobenzoate | HCID 18526058 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-fluoro-5-methoxy-4-nitrobenzoate | HCID 67076410 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Methyl 2,5-difluoro-4-nitrobenzoate (Apollo, 500 mg; 2.30 mmol; 1 eq.) was dissolved in MeOH (10 mL). The solution was cooled down to 0° C. Lithium bis(trimethylsilyl)amide (2.30 mL; 1 M; 2.30 mmol; 1 eq.) was added as solution in THF. After addition, the reaction mixture was stirred at RT overnight. Solvents were evaporated and the crude mixture was dissolved in EtOAc, washed with water, brine and dried over MgSO4. The resulting crude product was purified by flash chromatography (c-hex/EtOAc 90:10), affording the title product as a yellow solid. 1H NMR (CDCl3, 300 MHz) δ 7.60-7.52 (m, 2H), 3.93 (s, 3H), 3.91 (s, 3H). HPLC (Method A) Rt 3.88 min (Purity: 88.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202865B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-5d9cb3e83eeb4177bf8e89e7bfeb51e4 |
| Source note | uspto-grants-2012_06 |