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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251364Generated: November 2, 2026

Dibromomethane → 4-Bromo-1,3-benzodioxole

https://huagongshe.com/reaction/1251364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
Reactant1,2-Benzenediol, 3-bromo-HCID 26659—
ReactantPotassium FluorideHCID 522689—
SolventDimethylformamideHCID 6228—
Product4-Bromo-1,3-benzodioxoleHCID 277618945%

Reaction Conditions

Temperature135 °C

Reaction Steps

To 2,3-dihydroxy-bromobenzene (3.0 g, 0.16 mole), KF (4.63 g, 0.080 mole), DMF (15 mL was added CH2Br2 (4.13 g, 0.024 moles). This suspension was heated to 135° C. for 3 hours, cooled and filtered. The filtrate was poured into 200 mL of ether and washed with water, 1 N KOH and brine. The organic layer was dried over magnesium sulfate, filtered and the solvent removed under vacuum, to yield 2,3-Methylenedioxy-bromobenzene (1.45 g, 45 % yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342504B1
Source datasetuspto-grants-2002_01
ORD IDord-966e1995263f40bcb81f4af0d7c3253a
Source noteuspto-grants-2002_01