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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485771Generated: October 30, 2026

3,4-Dihydroxybenzaldehyde → 3,4-Bis[(3,4-dichlorophenyl)methoxy]benzaldehyde

https://huagongshe.com/reaction/485771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)-1,2-dichlorobenzeneHCID 639726—
SolventAcetoneHCID 180—
Product3,4-Bis[(3,4-dichlorophenyl)methoxy]benzaldehydeHCID 2024793684.1%

Reaction Steps

To a solution of 2 g of 3,4-dihydroxybenzaldehyde in 40 ml of acetone, were added 4.40 g of anhydrous potassium carbonate and 6.24 g of 3,4-dichlorobenzyl bromide. The mixture was refluxed for 24 hours. The reaction mixture was then removed of the acetone by distillation under reduced pressure, admixed with 200 ml of water, and the intended product was extracted with 200 ml of chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and stripped of the chloroform by distillation under reduced pressure to precipitate white crystals. The raw crystals were recrystallized from ethyl alcohol to give 4.99 g of colorless crystals having a melting point of 181°-183° C. The IR absorption spectrum of the compound, as measured in KBr-tablet, showed the following absorption maxima (in wave number, cm-1) 658, 693, 710, 760, 795, 805, 830, 875, 1030, 1135, 1168, 1200, 1245, 1280, 1370, 1403, 1437, 1460, 1470, 1510, 1585, 1600, 1690, 2730, 2830, 2870, 2910, and 3070.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537880
Source datasetuspto-grants-1985_08
ORD IDord-ead68e3688074f0d9b967b9bccc884a3
Source noteuspto-grants-1985_08