Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Bromo-5-fluoro-3-nitrobenzoic acid | HCID 18548583 | — |
| Product | HCID 20577071 | HCID 20577071 | 84% |
Reaction Steps
To the solution of 2-bromo-5-fluoro-3-nitrobenzoic acid (35 g) in MeOH (400 mL) was added SOCl2 (40 mL) drop-wise at 10-15° C. The reaction was then stirred at 65° C. for 1 h. After cooling to room temperature, the solvent was evaporated in vacuum to afford a residue, which was chromatographed on silica gel using gradient eluant of 0-100% EtOAc in hexane to provide methyl 2-bromo-5-fluoro-3-nitrobenzoate (20 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328111B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-67a2b8a66da548e8acde762fba7b729a |
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| Source note | uspto-grants-2016_05 |
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