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HRID 352737作成日:2026年10月25日

Hydrogen Bromide → 4-Bromo-2-hydroxybenzoic acid

https://huagongshe.com/reaction/352737

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物4-Aminosalicylic AcidHCID 4649—
反応物Ethyl AcetateHCID 8857—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
生成物4-Bromo-2-hydroxybenzoic acidHCID 268737—

反応条件

温度5 °C

反応手順

In water (22.5 ml) and a 47% aqueous solution of hydrobromic acid (22.5 ml), 4-amino-2-hydroxybenzoic acid (5.04 g) was dissolved. While the resulting solution mixture was maintained at 5° C. or lower, an aqueous solution (water: 15.0 ml) of sodium nitrite (2.26 g) was added dropwise thereto, followed by stirring for 30 minutes under ice cooling. The reaction mixture was added, in portions, to a solution of cuprous bromide (5.63 g) dissolved in a 47% aqueous solution of hydrobromic acid (15 ml) under ice cooling. The resulting mixture was stirred at room temperature for 150 minutes. Ethyl acetate was added to the reaction mixture for extraction. The organic layer so obtained was washed with water and then dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (dichloromethane˜10% methanol—dichloromethane), whereby 4-bromo-2-hydroxybenzoic acid (5.51 g) was obtained as a crudely purified product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747023B1
出典データセットuspto-grants-2004_06
ORD IDord-38308217afc74cc78456259a70ab092d
出典メモuspto-grants-2004_06