Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248556Generated: October 25, 2026

Dimethylformamide → 2-Methoxymethyloxy-4,5,6-trimethoxybenzaldehyde

https://huagongshe.com/reaction/248556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-Methoxymethyloxy-3,4,5-trimethoxyphenolHCID 67758527—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product2-Methoxymethyloxy-4,5,6-trimethoxybenzaldehydeHCID 20095708—

Reaction Steps

30.4 g of 1-methoxymethyloxy-3,4,5-trimethoxyphenol prepared in Referential Example 10 was dissolved in 250 ml of anhydrous ether, and 100 ml of n-butyllithium (1.6 M n-hexane solution) was dropwise added thereto at -20° C. After the completion of the dropwise addition, the mixture was stirred at room temperature for 2 hr, and 14.6 ml of DMF was added thereto. 100 ml of ice water was added thereto, and the mixture was extracted with ethyl acetate. The organic phase was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography (eluent; n-hexane ethyl acetate=6 : 4) to prepare 25.5 g of the product compound as a light yellow oleaginous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210239
Source datasetuspto-grants-1993_05
ORD IDord-6239c4899b33416ab49267d3315a3347
Source noteuspto-grants-1993_05