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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079140Generated: October 27, 2026

Hydrochloric Acid → 3,4-Dimethoxy-5-triisopropylsilanyloxymethylbenzaldehyde

https://huagongshe.com/reaction/2079140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant(5-Bromo-2,3-dimethoxybenzyloxy)triisopropylsilaneHCID 67097070—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3,4-Dimethoxy-5-triisopropylsilanyloxymethylbenzaldehydeHCID 59516888—

Reaction Steps

To a solution of the 3.616 g of (5-bromo-2,3-dimethoxybenzyloxy)triisopropylsilane in 60 ml of THF there was added dropwise 3.6 ml of n-butyllithium (2.66 M, hexane solution) at −78° C. under a nitrogen atmosphere. After stirring for 15 minutes, 2 ml of N-follnylmorpholine was added and the mixture was stirred at room temperature for 20 minutes. Next, 1N hydrochloric acid was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (2.605 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928228B2
Source datasetuspto-grants-2011_04
ORD IDord-1de46d39360745deae1fccc9b34c75b3
Source noteuspto-grants-2011_04