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HRID 989486作成日:2026年10月24日

Iodine → (+,-) Trans Propane-2-sulfonic Acid [2-(4-iodo-phenyl)-cyclopentyl]-amide

https://huagongshe.com/ja/reaction/989486

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Iodine pentoxideHCID 159402—
反応物(+,-) Trans-propane-2-sulfonic Acid (2-phenyl-cyclopentyl)-amideHCID 10956500—
反応物Sodium BisulfiteHCID 23665763—
溶媒Acetic AcidHCID 176—
生成物(+,-) Trans Propane-2-sulfonic Acid [2-(4-iodo-phenyl)-cyclopentyl]-amideHCID 11784171187.5%

反応条件

温度90 °C

反応手順

(+,−) Trans-propane-2-sulfonic acid (2-phenyl-cyclopentyl)-amide (0.52 g, 1.47 mmol, prepared in example 1) was dissolved in 30 mL of glacial acetic acid. To this solution was added concentrated sulfuric acid (0.16 mL, 1.61 mmol) at room temperature followed by iodine (0.19 g, 0.74 mmol), and diiodine pentoxide (0.20 g, 0.59 mmol). The reaction was then protected from light and heated to 90° C. and stirred for 22 hours. To the dark brown reaction mixture was slowly added 10% aqueous sodium bisulfite. The mixture was cooled to 0° C. for 1 hour and a light brown solid collected by filtration. The solid was dissolved in warm diethyl ether and washed with water (2×), then saturated sodium bicarbonate (1×). The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo to give 435 mg (75%) of the title compound. The NMR was consistent with the assigned structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06639107B1
出典データセットuspto-grants-2003_10
ORD IDord-1340a906f63c415a8cfb501561f1444f
出典メモuspto-grants-2003_10