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HRID 558434作成日:2026年10月27日

Trimethyl orthoformate → Ethyl 3-dimethoxymethyl-4-methoxybenzoate

https://huagongshe.com/reaction/558434

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl orthoformateHCID 9005—
反応物Sodium BicarbonateHCID 516892—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物Ethyl 3-formyl-4-methoxybenzoateHCID 638670—
溶媒MethanolHCID 887—
生成物Ethyl 3-dimethoxymethyl-4-methoxybenzoateHCID 2314141197%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063046B2
出典データセットuspto-grants-2011_11
ORD IDord-48dbf8b5698148bba2bc54c8f0b52c3a
出典メモuspto-grants-2011_11