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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13863생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Methyl-2-buteneHCID 10553—
반응물Methyl 4-formyl-3-methoxybenzoateHCID 10631650—
반응물Sodium ChloriteHCID 23668197—
용매DichloromethaneHCID 6344—
용매tert-ButanolHCID 6386—
생성물2-Methoxy-4-(methoxycarbonyl)benzoic acidHCID 5934033447%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728144B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b320caf1293a42f1b79feab23a43166c
출처 메모uspto-grants-2010_06