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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

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 numberUS06514996B2
Source datasetuspto-grants-2003_02
ORD IDord-7d65154f56be44c5b485c0d02beb4c0a
Source noteuspto-grants-2003_02