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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690605Generated: November 2, 2026

Water → 4-Methoxy-3-(3-methoxypropoxy)benzaldehyde

https://huagongshe.com/reaction/1690605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantIsovanillinHCID 12127—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-Methoxy-3-(3-methoxypropoxy)benzaldehydeHCID 1121835899.5%

Reaction Steps

3-hydroxy-4-methoxybenzaldehyde (15 g, 98.6 mmol) was dissolved in acetonitrile (200 mL). 1-Methoxy-3-bromopropane (16.6 g, 108 mmol) and potassium carbonate (34 g, 247 mmol) were added and the mixture was brought to reflux and stirred for 3 hrs. After cooling to room temperature, water and ethyl acetate were added. The aqueous layer was extracted three times with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to yield 22 g (quantitative yield) of the desired product as a yellow oil, used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153647B2
Source datasetuspto-grants-2012_04
ORD IDord-39c341f5ded94858a5f02a4f6d80ea2f
Source noteuspto-grants-2012_04