HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871856Generated: October 30, 2026
Methyl iodide → 1,5-Difluoro-3-methoxy-2-nitrobenzene
https://huagongshe.com/reaction/871856
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3,5-Trifluoro-2-nitrobenzene | HCID 67567 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,5-Difluoro-3-methoxy-2-nitrobenzene | HCID 10330129 | 95% |
Reaction Steps
To a solution of 2.45 g (14.0 mmol) of 1,3,5-trifluoro-2-nitrobenzene in acetone are successively added 2.9 g (21.0 mmol) of K2CO3 powder and 3.5 mL (56.0 mmol) of methyl iodide. The reaction mixture is heated at 50°C. for 2 hours and then filtered and evaporated to dryness. The residue is taken up in ethyl acetate and washed with water and with saturated aqueous NaCl solution. The organic phase is dried over Na2SO4, filtered and concentrated under vacuum. 2.52 g of the expected product are recovered in the form of a yellow solid, which is used as obtained in the following step. Yield=95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975250B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-9bc0aa9bb43c41db873da6befeb00ae8 |
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| Source note | uspto-grants-2015_03 |
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