Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976210Generated: October 30, 2026

Salicylaldehyde → 2-(3,5-Dimethoxybenzyloxy)benzaldehyde

https://huagongshe.com/reaction/1976210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant1-(Bromomethyl)-2,4-dimethoxybenzeneHCID 15151907—
SolventAcetoneHCID 180—
Product2-(3,5-Dimethoxybenzyloxy)benzaldehydeHCID 22000677—

Reaction Steps

Salicylaldehyde (0.32 cm3, 3.00 mmol), 4-bromomethyl-1,3-dimethoxybenzene (0.63 g, 2.73 mmol), potassium carbonate (0.42 g, 3.00 mmol), and 18-crown-6-ether (0.07 g, 0.27 mmol) were stirred together at room temperature in acetone (50 cm3, 99%) under nitrogen for 18 hours. The solution was evaporated under reduced pressure, and the residue was taken up in dichloromethane (20 cm3) and water (20 cm3). The aqueous layer was extracted with dichloromethane (2×20 cm3), and the combined extracts were washed with water (2×50 cm3), dried (MgSO4), and evaporated under reduced pressure. The residue was chromatographed (SiO2, heptane:ethyl acetate, 5:1) to give a white crystalline solid. The solid was recrystallized from heptane and ethyl acetate to give the ether, (0.58 g, 78%), as white fibrous needles, mp 68-69° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225352B1
Source datasetuspto-grants-2001_05
ORD IDord-289d003fae6a4932b41acf239015f16e
Source noteuspto-grants-2001_05