HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84935Generated: October 25, 2026
Methyl iodide → Benzoic acid, 2-bromo-5-fluoro-, methyl ester
https://huagongshe.com/reaction/84935
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-fluorobenzoic acid | HCID 2778181 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzoic acid, 2-bromo-5-fluoro-, methyl ester | HCID 138875 | — |
Reaction Steps
To a solution of 2-bromo-5-fluorobenzoic acid (7.92 g, 36.2 mmol) in N,N-dimethylformamide (75 mL) was added potassium carbonate (6.91 g, 50.0 mmol) as a solid in one portion at room temperature. The mixture was stirred for 5 minutes and iodomethane (6.39 g, 45.0 mmol) was added in one portion. The mixture was stirred at ambient temperature for 22 hours. The reaction mixture was partitioned between ethyl acetate and water. The aqueous portion was extracted with additional ethyl acetate (3×) and the combined organic extracts were washed successively with 10% potassium carbonate solution, water and brine. The organic portion was dried (Na2SO4) and concentrated to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 3.87 (s, 3H) 7.41 (td, J=8.56, 3.22 Hz, 1H) 7.65 (dd, J=8.99, 3.22 Hz, 1H) 7.81 (dd, J=9.16, 5.09 Hz, 1H); MS (+DCI/NH3) m/z 250.0 [M+NH4]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846951B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5de3b6ba492440bb930031c699186b10 |
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| Source note | uspto-grants-2014_09 |
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