HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955151Generated: October 26, 2026
Potassium Iodide → 4-(1,3-Benzodioxol-5-ylmethoxy)-2-hydroxybenzaldehyde
https://huagongshe.com/reaction/1955151
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2,4-Dihydroxybenzaldehyde | HCID 7213 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Benzodioxole, 5-(chloromethyl)- | HCID 88713 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 4-(1,3-Benzodioxol-5-ylmethoxy)-2-hydroxybenzaldehyde | HCID 10659762 | 31.4% |
Reaction Steps
A mixture of 2,4-dihydroxybenzaldehyde (22.94 g), 3,4-methylenedioxybenzyl chloride (34 g), potassium carbonate (34.43 g), potassium iodide (41.33 g) and tetra-n-butylammonium bromide (6 g) in methyl ethyl ketone was heated at reflux for 3 hours. The reaction mixture was filtered and evaporated. The residue was partitioned between ethyl acetate (400 ml) and water (400 ml) and the aqueous phase extracted twice with ethyl acetate (200 ml). The combined organic phases were dried over magnesium sulphate and evaporated. The residual beige coloured solid was purified by flash chromatography on silica eluting initially with a mixture of pentane and ethyl acetate (95:5, v/v) then with a mixture of pentane and ethyl acetate (9:1, v/v) and finally with a mixture of pentane and ethyl acetate (85:15, v/v). Fractions homogenous in the required product were combined and evaporated to give the title compound (14.2 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06124343 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-b79c81c3cf684614a4f099a4ec91d098 |
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| Source note | uspto-grants-2000_09 |
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