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HRID 1425441作成日:2026年10月27日

Trifluoroacetic acid → Ethyl 3-bromo-5-methylbenzoate

https://huagongshe.com/reaction/1425441

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Isoamyl NitriteHCID 8053—
反応物Phosphinic AcidHCID 4124402—
反応物Ethyl 2-amino-3-bromo-5-methylbenzoateHCID 54594338—
溶媒EthanolHCID 702—
生成物Ethyl 3-bromo-5-methylbenzoateHCID 2008662487.3%

反応手順

Ethanol (20 mL) was added to ethyl 2-amino-3-bromo-5-methylbenzoate obtained in Example (259d) (715 mg, 2.8 mmol). While the mixture was stirred, trifluoroacetic acid (0.82 mL, 11.1 mmol), isopentyl nitrite (649 mg, 5.5 mmol) and hypophosphorous acid (7.3 g, 55.4 mmol) were added under ice-cooling, followed by stirring at room temperature for 30 minutes. The reaction solution was diluted and extracted with ethyl acetate and aqueous sodium bicarbonate solution. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=0/10, 2/8) to obtain 594 mg of the title compound as a light yellow oily substance (88%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08927588B2
出典データセットuspto-grants-2015_01
ORD IDord-ac75a047d66c4d6f96284610698cedc7
出典メモuspto-grants-2015_01