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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248558Generated: October 30, 2026

Methyl iodide → 1-Methoxymethyloxy-2,3,4,5-tetramethoxybenzene

https://huagongshe.com/reaction/248558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxymethyloxy-4,5,6-trimethoxyphenolHCID 20095709—
SolventDimethylformamideHCID 6228—
Product1-Methoxymethyloxy-2,3,4,5-tetramethoxybenzeneHCID 13495532—

Reaction Conditions

Temperature45 °C

Reaction Steps

11.5 g of 2-methoxymethyloxy-4,5,6-trimethoxyphenol prepared in Referential Example 12 and 23.0 g of potassium carbonate were suspended in 100 ml of DMF. The suspension was heated at 45° C. while stirring, and 5.2 ml of iodomethane was dropwise added thereto. After the completion of the dropwise addition, the mixture was heated for 30 min, cooled and separated by filtration. 1 l of water was added to the mother liquor, 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=85 : 15) to prepare 6.2 g of the product compound as a colorless oleaginous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210239
Source datasetuspto-grants-1993_05
ORD IDord-e0a1f68cf8774c448a93bebdd1f00271
Source noteuspto-grants-1993_05