HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846505Generated: November 2, 2026
Methyl iodide → 1-Chloro-5-fluoro-2-methoxy-4-nitrobenzene
https://huagongshe.com/reaction/846505
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Chloro-5-fluoro-2-methoxy-4-nitrobenzene | HCID 2779295 | 76.4% |
Reaction Steps
To a stirred solution of 8.0 g (0.042 mole) of 2-chloro-4-fluoro-5-nitrophenol in 200 mL of acetone was added 6.09 g (0.0435 mole) of potassium carbonate. The mixture was heated at reflux temperature for 15 minutes, and 8.9 g (0.063 mole) of iodomethane was added. The resultant mixture was heated at reflux temperature for 5 hours, then stirred at room temperature for approximately 18 hours. The mixture was filtered and the filtrate evaporated under reduced pressure to leave a residue. The residue was dissolved in diethyl ether, filtered, and the filtrate washed with a saturated sodium chloride solution. The ether solution was dried over anhydrous sodium sulfate, filtered, and the filtrate evaporated to yield 6.6 g of 1-chloro-5-fluoro-2-methoxy-4-nitrobenzene as a solid, 63°-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05136868 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-4256073ea57c4139b0eefbdf6d0451b0 |
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| Source note | uspto-grants-1992_08 |
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