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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113549Generated: October 26, 2026

Hydrochloric Acid → 5-Methoxy-2-(3-methylbut-2-enyloxy)benzaldehyde

https://huagongshe.com/reaction/2113549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
Reactant2-Hydroxy-5-methoxybenzaldehydeHCID 95695—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Methoxy-2-(3-methylbut-2-enyloxy)benzaldehydeHCID 10584997—

Reaction Steps

To a solution of 2-hydroxy-5-methoxybenzaldehyde (7.6 g, 50 mmol) in dry N,N-dimethylformamide (100 mL) was added potassium carbonate (10.4 g), followed by 1-bromo-3-methylbut-2-ene (10.0 g, 67 mmol). The mixture was stirred at room temperature for 48 hours and ethyl acetate added. Sufficient 1M hydrochloric acid was cautiously added to neutralize the base, and the organic layer washed with water three times, followed by brine, and dried over magnesium sulfate. The mixture was filtered, and solvent removed from the filtrate under reduced pressure, to provide 5-methoxy-2-(3-methylbut-2-enyloxy)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432276B2
Source datasetuspto-grants-2008_10
ORD IDord-44283678dccd44feb4b01f19ab857d96
Source noteuspto-grants-2008_10