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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725584Generated: November 4, 2026

Vanillin → 3-Methoxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde

https://huagongshe.com/reaction/1725584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
SolventDimethylformamideHCID 6228—
Product3-Methoxy-4-[(4-methoxyphenyl)methoxy]benzaldehydeHCID 276449284.6%

Reaction Steps

A mixture of 4-hydroxy-3-methoxybenzaldehyde (22.6 g, 149 mmol), 4-methoxybenzyl chloride (23.3 g, 149 mmol) and potassium carbonate (30.8 g, 223 mmol) was stirred in N,N-dimethylformamide (DMF) (150 mL) at 90 C for 2 hours. The solution was filtered hot, and cooled to room temperature. The filtrate was concentrated and dissolved ethyl acetate (300 mL) and extracted with aqueous sodium bicarbonate and water. The organics were dried with magnesium sulfate, filtered and concentrated. The crude product was recrystalized with ethyl acetate and hexanes to give product as an off-white solid (34.2 g, 126 mmol). 1H NMR (300 MHz, d6-DMSO): δ 9.86 (s, 1H), 7.58 (d, J=8.2 Hz, 1H), 7.44-7.40 (m, 3H), 7.30 (d, J=8.4 Hz, 1H), 6.98 (d, J=8.7 Hz, 2H), 5.15 (s, 2H), 3.84 (s, 3H), 3.78 (s, 3H). MS (ES+, m/z)=273 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491731B2
Source datasetuspto-grants-2009_02
ORD IDord-bb4d26a59a30453c927d395d4d645b4f
Source noteuspto-grants-2009_02