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HRID 596054作成日:2026年10月25日

Iodine → 4-Chloro-2-fluoro-6-iodobenzoic acid

https://huagongshe.com/reaction/596054

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物DimethylformamideHCID 6228—
反応物4-Chloro-2-fluorobenzoic acidHCID 99152—
反応物Iodo benzene diacetateHCID 12217721—
触媒palladium(II) acetateHCID 167845—
溶媒Ethyl AcetateHCID 8857—
生成物4-Chloro-2-fluoro-6-iodobenzoic acidHCID 118045935—

反応条件

温度100 °C

反応手順

To a 250 mL flask were added 4-chloro-2-fluorobenzoic acid (4 g, 22.92 mmol), Pd(OAc)2 (0.257 g, 1.146 mmol), iodobenzene diacetate (8.12 g, 25.2 mmol), iodine (6.40 g, 25.2 mmol) and DMF (60 mL). The solution was heated under a nitrogen atmosphere at 100° C. for 20 h. LCMS showed about half of 4-chloro-2-fluorobenzoic acid was converted to the product (LCMS retention time 0.98 min, no MH+ peak). After cooling to room temperature, the solution was diluted with EtOAc and washed three times with 1 N HCl. The aqueous layers were combined and extracted once with EtOAc. The organic layers were combined, dried over Na2SO4 and concentrated to give a dark brown oil (16.4 g, 42% pure), which was taken to the next step without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242996B2
出典データセットuspto-grants-2016_01
ORD IDord-3f19965fe351414d9c0e744a7d758022
出典メモuspto-grants-2016_01