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HRID 393001作成日:2026年10月25日

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

https://huagongshe.com/reaction/393001

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 1867300387%

反応条件

温度83 °C

反応手順

A mixture of 4-bromo-2-methylbenzoic acid, methyl ester (22.59 g, 98.6 mmol), triethylamine (32.00 g, 316.2 mmol), palladium(II) acetate (0.56 g, 2.5 mmol), bis(diphenylphosphino)propane (1.04 g, 2.5 mmol) and water (32 mL, 1776.3 mmol) in acetonitrile (80 mL) was pressurized to 40 psi 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 (200 mL) was added. The solution was filtered and then extracted with water (2×300 mL). The combined aqueous layers were acidified with 12 M HCl to pH 0. The resulting mixture was extracted with ethyl acetate (2×300 mL). The combined organic layers were dried (MgSO4), filtered and evaporated to give 2-methylbenzene-1,4-dicarboxylic acid 1-methyl ester (16.57 g, 87%) as a white solid, mp 134-136° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06803384B2
出典データセットuspto-grants-2004_10
ORD IDord-8d067f3f8e6544aa9eafb362d3fde711
出典メモuspto-grants-2004_10