HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057945Generated: October 26, 2026
Water → 6-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepin
https://huagongshe.com/reaction/1057945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 3-Bromo-6-methoxybenzene-1,2-diol | HCID 3705874 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepin | HCID 23272337 | — |
Reaction Steps
3-bromo-6-methoxycatechol (31 g) was dissolved in DMF (50 ml), mixed with 1,3-dibromopropane (36 ml) and potassium fluoride (42 g), stirred for 12 hours while heating at 110° C. The resultant was allowed to stand for cooling, mixed with water, and extracted with ether. The organic layer was washed with an aqueous sodium hydroxide solution, water, and a saturated aqueous sodium chloride solution in that order, dried over manganese sulfate, and evaporated under reduced pressure for removing the solvent. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to give Compound IIbr-a (6.7 g, 18%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06514996B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-7d65154f56be44c5b485c0d02beb4c0a |
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| Source note | uspto-grants-2003_02 |
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