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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084827Generated: October 27, 2026

Water → 6-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepin

https://huagongshe.com/reaction/2084827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium FluorideHCID 522689—
Reactant3-Bromo-6-methoxybenzene-1,2-diolHCID 3705874—
SolventDimethylformamideHCID 6228—
Product6-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepinHCID 23272337—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716987B1
Source datasetuspto-grants-2004_04
ORD IDord-b085775180fb4db182c339eea535ffe8
Source noteuspto-grants-2004_04