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HRID 279538作成日:2026年10月26日

5-Amino-4-fluoro-2-methylphenyl Methoxyformate → (4-Fluoro-5-hydroxy-2-methylphenyl) methyl carbonate

https://huagongshe.com/reaction/279538

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-4-fluoro-2-methylphenyl MethoxyformateHCID 22625046—
反応物Sodium NitriteHCID 23668193—
触媒Copper oxideHCID 14829—
触媒Copper(II) nitrate trihydrateHCID 9837674—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
生成物(4-Fluoro-5-hydroxy-2-methylphenyl) methyl carbonateHCID 2262503153.2%

反応条件

温度0 °C

反応手順

A solution of sodium nitrite (1.63 g, 23 mmol) in water (19 ml) and ice (48 g) was added dropwsie to a solution of 2-fluoro-5-methoxycarbonyloxy-4-methylaniline (3.93 g, 20 mmol) in 35% sulphuric acid (48 ml) at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes and a solution of copper(II)nitrate trihydrate (467 g, 1.93 mol) in water (780 ml) followed by copper(II)oxide (2.65 g, 18 mmol) were added. The solution was extracted with ethyl acetate, the organic layer was washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with petroleum ether/ethyl acetate (8/2) to give 2-fluoro-5-methoxycarbonyloxy-4-methylphenol (2.13 g, 53%) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362336B1
出典データセットuspto-grants-2002_03
ORD IDord-e70dd8e5684847159b21a5e6e481d2f3
出典メモuspto-grants-2002_03