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HRID 1058388作成日:2026年10月27日

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

https://huagongshe.com/reaction/1058388

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物Ethyl AcetateHCID 8857—
反応物Methyl 4-bromo-2-methylbenzoateHCID 22031226—
反応物HCID 178418416HCID 178418416—
触媒palladium(II) acetateHCID 167845—
触媒Phosphine, (1-methylethylidene)bis[diphenyl-HCID 12091099—
溶媒AcetonitrileHCID 6342—
生成物4-(Methoxycarbonyl)-3-methylbenzoic acidHCID 1867300347%

反応条件

温度83 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06515124B2
出典データセットuspto-grants-2003_02
ORD IDord-1b88ce79cbd944b2b96dd51dc7c43e6a
出典メモuspto-grants-2003_02