戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 541070作成日:2026年10月27日

Triethylamine → N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamide

https://huagongshe.com/reaction/541070

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物Methanesulfonyl chlorideHCID 31297—
反応物2-Iodo-4-nitroanilineHCID 222629—
溶媒DichloromethaneHCID 6344—
生成物N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamideHCID 6728434480.2%

反応手順

To a solution containing 2-iodo-4-nitroaniline (25 g; 95 mmol) and triethylamine (43 ml; 312 mmol) in CH2Cl2 (250 ml), a solution containing methanesulphonyl chloride (36 g; 312 mmol) was added dropwise. The reaction mixture was left under stirring at room temperature for 18 hours, then NH4Cl (saturated solution) was added (250 ml). The biphasic solution was transferred into a separating funnel, the organic phase was separated, dried over Na2SO4 and the solvent was removed by evaporation under reduced pressure. The residue was suspended in EtOH (200 ml) and heated under stirring until a yellow solid precipitated. The crude product was filtered, washed with EtOH (750 ml), and dried under vacuum to give N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamide (32 g) which was used in the following reaction without any further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871948B2
出典データセットuspto-grants-2014_10
ORD IDord-6a22ef69760549eb857c99282f72fc4f
出典メモuspto-grants-2014_10