HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497029Generated: October 26, 2026
Dimethylformamide → 8-Methoxy-2,3-dihydro-1,4-benzodioxine-6-carbaldehyde
https://huagongshe.com/reaction/497029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4-Dihydroxy-5-methoxybenzaldehyde | HCID 77535 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-Methoxy-2,3-dihydro-1,4-benzodioxine-6-carbaldehyde | HCID 606578 | 43% |
Reaction Steps
In a vial was placed 0.5 g (3.0 mmol) of 3,4-dihydroxy-5-methoxybenzaldehyde, 414 mg (3.0 mmol) of K2CO3, and 3 mL of anhydrous DMF. To this mixture was added, 0.56 g (3.0 mmol) of 1,2-dibromoethane dropwise. The vial was sealed and heated to 100° C. overnight. Water was added to the reaction and the mixture was extracted with diethyl ether. The organic extract was washed with brine, dried (Na2SO4), filtered, and concentrated to give the crude product. The material was purified by silica gel chromatography using 50% ethyl acetate/hexane as the eluent to afford 0.25 g (43%) of the pure aldehyde 10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949544B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-a4782987aa6047e68ec8565ac771b778 |
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| Source note | uspto-grants-2005_09 |
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