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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2,4-DihydroxybenzaldehydeHCID 7213—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Benzodioxole, 5-(chloromethyl)-HCID 88713—
CatalystTetrabutylammonium BromideHCID 74236—
SolventMethyl Ethyl KetoneHCID 6569—
Product4-(1,3-Benzodioxol-5-ylmethoxy)-2-hydroxybenzaldehydeHCID 1065976231.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124343
Source datasetuspto-grants-2000_09
ORD IDord-b79c81c3cf684614a4f099a4ec91d098
Source noteuspto-grants-2000_09