HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37547Generated: October 26, 2026
Dichloromethane → 1,3-Benzodioxole-4-carboxaldehyde
https://huagongshe.com/reaction/37547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dihydroxybenzaldehyde | HCID 90579 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Benzodioxole-4-carboxaldehyde | HCID 82264 | 80% |
Reaction Steps
138.0 g (1.0 mol) of 2,3-dihydroxybenzaldehyde, 415.0 g (3.0 mol) of potassium carbonate, 4.7 g of copper oxide, 255.0 g (3.0 mol) of methylene chloride and 1500 ml of distilled dimethylformamide are boiled for 7 hours, while stirring intensively.. The reaction mixture is evaporated to dryness in vacuo and, after addition of 1000 ml of ice-water to the residue, the mixture is extracted four times by shaking with 300 ml of methyl tert-butyl ether each time. The combined ether extracts are washed with 5% strength sodium hydroxide solution and water and dried over sodium sulphate. The methyl tert-butyl ether is then stripped off (and can be reused) and the residue is distilled in vacuo at 92°-93° C./1 mbar. 120 g (80% of theory) of 2,3-methylenedioxybenzaldehyde having a melting point of 32°-33° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05420308 |
|---|
| Source dataset | uspto-grants-1995_05 |
|---|
| ORD ID | ord-4b98333f616c4365be8428d1d25e105a |
|---|
| Source note | uspto-grants-1995_05 |
|---|