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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156444Generated: October 30, 2026

Dibromomethane → 1,3-Benzodioxole, 5-methyl-

https://huagongshe.com/reaction/1156444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
Reactant4-MethylcatecholHCID 9958—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product1,3-Benzodioxole, 5-methyl-HCID 8156489%

Reaction Steps

Alternatively, a solution composed of 0.7 mol of the compound (V) obtained by the above process, 1.75 mols of sodium hydroxide, and a 2.8-fold amount by weight, based on (V), of water was added dropwise to a solution composed of a 1.6-fold amount by weight, based on (V), of water, 2.0 mols of dibromomethane, and 0.007 mol of tetra-n-butylammonium bromide over 5 hours under reflux condition. After completion of the dropwise addition, the mixture was maintained at the same temperature for 2 hours while stirring. After completion of the reaction, the reaction mixture was extracted with toluene and, after liquid separation, the toluene was distilled off from the resulting organic layer. Distillation of the residue gave 3,4-methylenedioxytoluene (VI-1) in 89% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335263
Source datasetuspto-grants-1982_06
ORD IDord-79a00de264ce45a2b4e3e4a6e4ea628d
Source noteuspto-grants-1982_06