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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404689Generated: November 1, 2026

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

https://huagongshe.com/reaction/1404689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantMethyl 4-formyl-3-methoxybenzoateHCID 10631650—
ReactantSodium ChloriteHCID 23668197—
SolventDichloromethaneHCID 6344—
Solventtert-ButanolHCID 6386—
Product2-Methoxy-4-(methoxycarbonyl)benzoic acidHCID 5934033447%

Reaction Steps

To a stirred solution of 4-formyl-3-methoxy-benzoic acid methyl ester (5.0 g, 26 mmol) 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 product, 2-methoxyterephthalic acid 4-methyl ester, was obtained in 47% yield (2.4 g, 12.3 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912334B2
Source datasetuspto-grants-2014_12
ORD IDord-90c26fc02737446abfd5b5d398563c79
Source noteuspto-grants-2014_12