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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646390Generated: November 1, 2026

Trimethyl orthoformate → Ethyl 3-dimethoxymethyl-4-methoxybenzoate

https://huagongshe.com/reaction/646390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantEthyl 3-formyl-4-methoxybenzoateHCID 638670—
SolventMethanolHCID 887—
ProductEthyl 3-dimethoxymethyl-4-methoxybenzoateHCID 2314141197%

Reaction Steps

Ethyl 3-formyl-4-methoxybenzoate (500 mg) obtained in step C of Example 1-2-1 was dissolved in 10 mL of methanol. Trimethyl orthoformate (263 μL) and 41 mg of p-toluenesulfonic acid monohydrate were added to the solution, and then the mixture was heated for 2 hours under reflux. After the reaction solution was cooled, 5 mL of a saturated aqueous solution of sodium bicarbonate was added, and the resulting mixture was concentrated under reduced *pressure. The residue was diluted with ethyl acetate, washed with purified water and then with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was separated by filtration, whereafter the filtrate was concentrated under reduced pressure. The residue was dried under reduced pressure to obtain 596 mg (97%) of ethyl 3-dimethoxymethyl-4-methoxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705053B2
Source datasetuspto-grants-2010_04
ORD IDord-eab6a91e5c704e30a17f09bf468395f3
Source noteuspto-grants-2010_04