戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2254668作成日:2026年10月27日

Iodine → N-(4-iodo-3-methylphenyl)-N-methylmethanesulphonamide

https://huagongshe.com/reaction/2254668

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Iodic acidHCID 24345—
反応物Sodium BicarbonateHCID 516892—
反応物N-Methyl-N-(3-tolyl)methanesulphonamideHCID 19785598—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Sulfuric AcidHCID 1118—
溶媒Ethyl AcetateHCID 8857—
生成物N-(4-iodo-3-methylphenyl)-N-methylmethanesulphonamideHCID 19785617340%

反応手順

A solution of N-methyl-N-(3-tolyl)methanesulphonamide (0.12 g), iodine (76 g) and iodic acid (35 mg) in glacial acetic acid (5 ml) and concentrated sulphuric acid (0.6 ml) was stirred at 80° C. for 2.5 hours. Ethyl acetate (40 ml) and water (40 ml) were then added and the mixture neutralised with solid sodium bicarbonate. The organic phase was washed with brine (30 ml), dried (MgSO4) and the solvent evaporated to leave N-(4-iodo-3-methylphenyl)-N-methylmethanesulphonamide (0.22 g, 90%), m.p. 85°-87° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05236948
出典データセットuspto-grants-1993_08
ORD IDord-2ef0909f59a044baa0c31e4730d78f1d
出典メモuspto-grants-1993_08