HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069487Generated: October 27, 2026
Dibromomethane → 1,3-Benzodioxole, 6-bromo-4-methoxy-
https://huagongshe.com/reaction/1069487
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-3-methoxybenzene-1,2-diol | HCID 10987756 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Benzodioxole, 6-bromo-4-methoxy- | HCID 10911396 | 52% |
Reaction Steps
To dimethylformamide (400 mL) was added 1-bromo-3,4-dihydroxy-5-methoxybenzene (40 g, 182 mmol), potassium carbonate (75.7 g, 548 mmol), and dibromomethane (95.2 g, 548 mmol), followed by heating to reflux for 1 hour. The solvent was evaporated in vacuo, and the residue was taken up into ethyl ether, filtered, washed with saturated potassium carbonate solution, brine, 1N citric acid solution, and brine. The organic phase was dried over anhydrous magnesium sulfate and filtered through charcoal. The filtrate was concentrated in vacuo giving a crystalline precipitate which was filtered, washed with hexane, and dried in vacuo to a solid. This material was distilled at 2 mm Hg, 125° C., giving a crystalline solid, 21.7 g, 52% yield. NMR spectra and elemental analysis were consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06252070B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-33add3b8bb9444f4bc4bd705b53c3c86 |
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| Source note | uspto-grants-2001_06 |
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