HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079165Generated: October 27, 2026
Sodium Iodide → 4H-1,3-Benzodioxin, 5-fluoro-8-methoxy-
https://huagongshe.com/reaction/2079165
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Bromochloromethane | HCID 6333 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Fluoro-2-hydroxymethyl-6-methoxyphenol | HCID 67096966 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4H-1,3-Benzodioxin, 5-fluoro-8-methoxy- | HCID 59517458 | — |
Reaction Steps
To a solution of the 6.1 g of 3-fluoro-2-hydroxymethyl-6-methoxyphenol in 90 ml of DMF there was added 3 g of sodium hydride (60% oily suspension) while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After adding 2.55 ml of bromochloromethane and 510 mg of sodium iodide to the reaction mixture, it was stirred at 80° C. for 6 hours under a hydrogen atmosphere. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (1.086 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928228B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-4f6eea71315a46a89510274bb7cf3809 |
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| Source note | uspto-grants-2011_04 |
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