HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499685Generated: October 31, 2026
Methyl iodide → 1-(5-Chloro-4-fluoro-3-iodo-2-methoxyphenyl)ethanone
https://huagongshe.com/reaction/1499685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(5-Chloro-4-fluoro-2-hydroxy-3-iodophenyl)ethanone | HCID 86666857 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(5-Chloro-4-fluoro-3-iodo-2-methoxyphenyl)ethanone | HCID 86666858 | 74.2% |
Reaction Steps
1-(5-Chloro-4-fluoro-2-hydroxy-3-iodophenyl)ethanone (13 g, 41 mmol) was dissolved in N,N-dimethylformamide (41.3 mL). Methyl iodide (3.9 mL, 62 mmol) was added followed by potassium carbonate (11 g, 83 mmol). The reaction was heated at 60° C. for 1 hour. The mixture was cooled to room temperature, diluted with ether. The organic layers were separated and combined, washed with water, dried over MgSO4, concentrated and purified on silica gel (eluting with 0 to 10% EtOAc in hexanes) to give the desired product (10 g, 70%). LCMS calculated for C9H8ClFIO2 (M+H)+: m/z=328.9; Found: 328.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199982B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-c27bd1c44c4b44c58c937a37a7ae7387 |
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| Source note | uspto-grants-2015_12 |
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