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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13863Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/13863

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2-Methyl-2-buteneHCID 10553—
EduktMethyl 4-formyl-3-methoxybenzoateHCID 10631650—
EduktSodium ChloriteHCID 23668197—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmitteltert-ButanolHCID 6386—
Produkt2-Methoxy-4-(methoxycarbonyl)benzoic acidHCID 5934033447%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728144B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b320caf1293a42f1b79feab23a43166c
Quellennotizuspto-grants-2010_06