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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505661Generated: October 31, 2026

Methanol → 2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/505661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant2-Bromo-1-(benzyloxymethyl)-3,5-bis(methoxymethoxy)benzeneHCID 23147594—
SolventDiethyl EtherHCID 3283—
Product2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehydeHCID 2166981772%

Reaction Conditions

Temperature-78 °C

Reaction Steps

The above-obtained 2-bromo-1-(benzyloxymethyl)-3,5-bis(methoxymethoxy)benzene (1.6 g, 4.3 mmol) was dissolved in diethylether (25 mL) and cooled to −78° C. The obtained solution was added with 1.52 mol/L n-butyllithium-hexane solution (4.0 mL, 6.1 mmol) and stirred at −78° C. for 1 hour. Then, N,N-dimethylformamide (1.0 mL, 13 mmol) was added thereto and stirred at a room temperature for 3 hours. The reaction mixture was added with water and methanol, and then extracted with chloroform 3 times. The organic layers were combined, washed with saturated brine, and then dried over anhydrous sodium sulfate. Then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1 to 5/1 to 3/1) to obtain 2-(benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde (0.99 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781485B2
Source datasetuspto-grants-2010_08
ORD IDord-4f6fedc485ba409ca1005d609e123232
Source noteuspto-grants-2010_08