HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370355Generated: October 31, 2026
Methyl iodide → 4-Bromo-2-fluoro-1-(methoxymethyl)benzene
https://huagongshe.com/reaction/2370355
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (4-Bromo-2-fluorophenyl)methanol | HCID 2734027 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-2-fluoro-1-(methoxymethyl)benzene | HCID 21647637 | 83.2% |
Reaction Steps
The title compound was prepared according to General Method 8. To a suspension of NaH (50-60% mineral oil, 8 g, 0.33 mol) in Dry DMF (200 mL) at 0° C. was added (4-bromo-2-fluorophenyl)methanol (27 g, 0.1317 mol). The reaction mixture was stirred for 15 min at 0° C. and then warmed to and stirred at RT for 30 min. The reaction mixture was again cooled to 0° C. and MeI (15 mL, 0.1975 mol) was added drop wise. After addition was complete, the reaction mixture was warmed to room temperature and stirred for 1 h. Ice-water was added and the product was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate, and concentrated under reduced pressure to obtained 4-bromo-2-fluoro-1-(methoxymethyl)benzene (24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710086B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-cf7e13297d3b46ebbd3de80c7ab6ca47 |
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| Source note | uspto-grants-2014_04 |
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