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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 541070생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/541070

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ammonium ChlorideHCID 25517—
반응물Methanesulfonyl chlorideHCID 31297—
반응물2-Iodo-4-nitroanilineHCID 222629—
용매DichloromethaneHCID 6344—
생성물N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamideHCID 6728434480.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871948B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-6a22ef69760549eb857c99282f72fc4f
출처 메모uspto-grants-2014_10