HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156444Generated: October 30, 2026
Dibromomethane → 1,3-Benzodioxole, 5-methyl-
https://huagongshe.com/reaction/1156444
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | 4-Methylcatechol | HCID 9958 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Benzodioxole, 5-methyl- | HCID 81564 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04335263 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-79a00de264ce45a2b4e3e4a6e4ea628d |
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| Source note | uspto-grants-1982_06 |
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