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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305342Generated: October 31, 2026

Dibromomethane → 1,3-Benzodioxole, 6-bromo-4-methoxy-

https://huagongshe.com/reaction/2305342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-3-methoxybenzene-1,2-diolHCID 10987756—
SolventDimethylformamideHCID 6228—
Product1,3-Benzodioxole, 6-bromo-4-methoxy-HCID 1091139652%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06440962B2
Source datasetuspto-grants-2002_08
ORD IDord-7c5c25689f3b441a9cc2269961059555
Source noteuspto-grants-2002_08