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HRID 1070477作成日:2026年10月25日

Iodine → Methyl 5-chloro-4-iodo-2-methoxybenzoate

https://huagongshe.com/reaction/1070477

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Sulfuric AcidHCID 1118—
反応物Potassium IodideHCID 4875—
反応物Methyl 4-amino-5-chloro-2-methoxybenzoateHCID 700493—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
生成物Methyl 5-chloro-4-iodo-2-methoxybenzoateHCID 6931479584.2%

反応条件

温度-1 °C

反応手順

4-Amino-5-chloro-2-methoxy benzoic acid methyl ester of Step A (5.00 g, 23.2 mmol) was suspended in water (52 mL) and concentrated sulfuric acid (13 mL) was added. The resulting suspension was cooled to −1° C. and a solution of sodium nitrite (1.76 g, 25.5 mmol) in water (10 mL) was added at a rate which maintained the temperature below 0° C., resulting in the formation of a clear yellow solution. A mixture of potassium iodide (4.23 g, 25.5 mmol) and iodine (3.24 g, 12.8 mmol) in water (50 mL) was then added dropwise and the reaction stirred at 0° C. for 1.5 hours. The reaction mixture was warmed to room temperature and extracted with ethyl acetate (200 mL). The combined extracts were washed sequentially with 1 M aqueous sodium thiosulfate, 1 N sodium hydroxide and brine, and dried over anhydrous magnesium sulfate, filtered and concentrated, whereupon the product crystallized. The resulting orange crystals were suspended in petroleum ether, filtered and dried in vacuo to provide the title compound (6.38 g), m.p. 72-73° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06903087B2
出典データセットuspto-grants-2005_06
ORD IDord-eca0e913ea50458f932cf24f936703ed
出典メモuspto-grants-2005_06