HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404352Generated: October 28, 2026
Dimethylformamide → Methyl 2'-fluoro-5'-(methyloxy)-2-nitro-1,1'-biphenyl-4-carboxylate
https://huagongshe.com/reaction/404352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 4-chloro-3-nitrobenzoate | HCID 735797 | — |
| Reactant | 2-Fluoro-5-methoxyphenylboronic acid | HCID 4157211 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Methyl 2'-fluoro-5'-(methyloxy)-2-nitro-1,1'-biphenyl-4-carboxylate | HCID 57706335 | 99.7% |
Reaction Steps
To a stirred solution of methyl 4-chloro-3-nitrobenzoate T20.1 (10.00 g, 46 mmol) (commercially available from Sigma-Aldrich, St. Louis, Mo., USA) in DMF (15.00 mL, 194 mmol) at 23° C. was added 2-fluoro-5-methoxyphenylboronic acid (12 g, 70 mmol) (commercially available from Sigma-Aldrich, St. Louis, Mo., USA), and potassium carbonate (19 g, 139 mmol). Tetrakis(triphenylphosphine)palladium (2.1 g, 1.9 mmol) was then added to the mixture, and the mixture was heated at 90° C. for 18 hours. The mixture was then cooled to room temperature, diluted with brine and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was purified on silica gel (0-40% EtOAc in hexanes) to yield T20.2 as a colorless oil (14.00 g, 99% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748462B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-c72ebf4d9431432ba8136ca67ae5d721 |
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| Source note | uspto-grants-2014_06 |
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