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HRID 14291作成日:2026年10月25日

Hydrochloric Acid → 3-Iodo-5-(methoxycarbonyl)benzoic acid

https://huagongshe.com/reaction/14291

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium IodideHCID 4875—
反応物3-Amino-5-(methoxycarbonyl)benzoic acidHCID 13557643—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
生成物3-Iodo-5-(methoxycarbonyl)benzoic acidHCID 1584039155.1%

反応手順

To an ice-cold, stirred solution of 3-amino-5-(methoxycarbonyl)benzoic acid (5.19 g, 26.59 mmol) in a 2 N hydrochloric acid (156 mL) was added a solution of sodium nitrite (1.84 g, 26.67 mmol) in water (10.8 mL). This mixture was then added dropwise to an ice-cold, stirred solution of potassium iodide (8.84 g, 53.25 mmol) in water (26.2 mL). After stirring for 35 min, the reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with 5% aqueous sodium thiosulfate, and saturated sodium chloride, dried (sodium sulfate), and concentrated under reduced pressure. Purification by flash column chromatography (silica, 50:50:2 hexanes/ethyl acetate/acetic acid) afforded 3-iodo-5-(methoxycarbonyl)benzoic acid (4.48 g): 1H NMR (500 MHz, DMSO-d6): δ 13.49 (br s, 1H), 8.45-8.38 (m, 3H), 3.83 (s, 3H); ESI-MS (m/z): 305 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-b9e365e738df4d5f94ed7d7af91e7e2d
出典メモuspto-grants-2010_06