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HRID 7495作成日:2026年10月24日

5-Benzyloxy-2-fluoro-4-methylaniline → 5-Benzyloxy-2-fluoro-4-methylphenol

https://huagongshe.com/ja/reaction/7495

反応式

関与物質

役割名称HCID仕込み量
反応物5-Benzyloxy-2-fluoro-4-methylanilineHCID 21991068—
反応物Sodium NitriteHCID 23668193—
触媒Copper oxideHCID 14829—
触媒Copper(II) nitrate trihydrateHCID 9837674—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
生成物5-Benzyloxy-2-fluoro-4-methylphenolHCID 2199104927%

反応手順

The starting material 5-benzyloxy-2-fluoro-4-methylphenol, was obtained by adding a solution of sodium nitrite (1.68 g, 24mmol) in water (3.5 ml), dropwise, to a solution of 5-benzyloxy-2-fluoro-4-methylaniline (4.7 g, 20 mmol) in acetic acid (82 ml) and 70% sulphuric acid (3.15 ml) cooled at 10° C. The mixture was stirred vigorously for 20 minutes, then a solution of copper(II)nitrate trihydrate (481 g, 2 mol) in water (790 ml) was added, followed by copper(II)oxide (3 g, 19 mmol). After stirring for 3 hours, the mixture was extracted with ethyl acetate. The organic layer was washed with water and then brine, dried (MgSO4) and the solvent evaporated. The resulting oil was purified by flash chromatography using petroleum ether/ether (85/15) as eluent to give 5-benzyloxy-2-fluoro-4-methylphenol as an orange oil (1.25 g, 27%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087602B2
出典データセットuspto-grants-2006_08
ORD IDord-051c546095a445e08c053b9eb100de40
出典メモuspto-grants-2006_08