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HRID 13863作成日:2026年10月25日

Water → 2-Methoxy-4-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/13863

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-Methyl-2-buteneHCID 10553—
反応物Methyl 4-formyl-3-methoxybenzoateHCID 10631650—
反応物Sodium ChloriteHCID 23668197—
溶媒DichloromethaneHCID 6344—
溶媒tert-ButanolHCID 6386—
生成物2-Methoxy-4-(methoxycarbonyl)benzoic acidHCID 5934033447%

反応手順

To a stirred solution of 4-formyl-3-methoxybenzoic acid methyl ester (5.0 g, 26 mmol; prepared as described in Preparation 17) in tert-butyl alcohol (200 mL) was added NaH2PO4-2H2O (3.6 g, 26 mmol), water (50 mL), 2-methyl-2-butene (11 mL, 104 mmol), and finally NaClO2 (7.02 g, 78 mmol). The reaction was allowed to stir at room temperature for 4 hours. The solvent was then removed under reduced pressure. The crude reaction mixture was then dissolved in DCM (200 mL) and the product was extracted with 1N NaOH (200 mL). The aqueous layer was washed with DCM (200 mL) and then neutralized with 6N HCl (˜40 mL) and the product extracted with DCM (200 mL). The organic layer was then washed with water (100 mL), NaCl (sat.) (100 mL), dried over MgSO4 and then filtered. The solvent was removed under reduced pressure. The crude material was sufficiently pure to use without further purification. The title intermediate was obtained in 47% yield (2.4 g, 12.3 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728144B2
出典データセットuspto-grants-2010_06
ORD IDord-b320caf1293a42f1b79feab23a43166c
出典メモuspto-grants-2010_06