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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1058388생성일: 2026년 10월 27일

Water → 4-(Methoxycarbonyl)-3-methylbenzoic acid

https://huagongshe.com/reaction/1058388

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물Methyl 4-bromo-2-methylbenzoateHCID 22031226—
반응물HCID 178418416HCID 178418416—
촉매palladium(II) acetateHCID 167845—
촉매Phosphine, (1-methylethylidene)bis[diphenyl-HCID 12091099—
용매AcetonitrileHCID 6342—
생성물4-(Methoxycarbonyl)-3-methylbenzoic acidHCID 1867300347%

반응 조건

온도83 °C

반응 단계

A mixture of 4-bromo-2-methylbenzoic acid methyl ester (prepared by the literature method: Keuning, K. J.; Evenhuis, N. Recueil Trav. Chim. Pays-Bas 1935, 54, 73-75; 12.21 g, 53.3 mmol), triethylamine (16.00 g, 158.1 mmol), palladium(II) acetate (0.28 g, 1.25 mmol), bis(diphenylphosphino)propane (0.52 g, 1.26 mmol), water (16.00 g, 888.1 mmol) and acetonitrile (40 mL) was pressurized to 40 pounds per square inch with carbon monoxide and the pressure was released. After six such cycles, the bottle was pressurized again and the contents were stirred at 83° C. for 3 h. The reaction mixture was cooled to room temperature and depressurized. Ethyl acetate (100 mL) was added and the solution was filtered and then extracted with water (5×40 mL). The combined aqueous layers were acidified with 1N hydrochloric acid solution to pH 2 and the resulting mixture was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with brine (200 mL), dried (MgSO4) and evaporated under reduced pressure to give 4-(methoxycarbonyl)-3-methylbenzoic acid as a colorless solid (4.83 g, 47% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06515124B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-1b88ce79cbd944b2b96dd51dc7c43e6a
출처 메모uspto-grants-2003_02