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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 421522생성일: 2026년 10월 26일

4-Toluenesulfonyl chloride → N,N-bis(2-chloroethyl)-p-toluenesulphonamide

https://huagongshe.com/reaction/421522

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물TriethylamineHCID 8471—
반응물Bis(2-chloroethyl)amine hydrochlorideHCID 522769—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TetrahydrofuranHCID 8028—
생성물N,N-bis(2-chloroethyl)-p-toluenesulphonamideHCID 9603980.1%

반응 단계

To a suspension of bis(2-chloroethyl)amine hydrochloride (4.68 g, 26.2 mmol) in dry THF (50 mL) was added Et3N (18.3 mL, 131 mmol) at 0° C. and the mixture was stirred for 15 min. p-Toluenesulfonyl chloride (5.00 g, 26.25 mmol) and DMAP (a spatula pinch) were added. The reaction mixture was allowed to warm to room temperature and was stirred overnight. When TLC analysis showed complete conversion, the mixture was filtered to remove the Et3N.HCl and extracted with EtOAc. The combined organic phases were washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash column chromatography to afford N,N-bis(2′-chloroethyl)-4-methylbenzenesulfonamide (6.22 g, 80% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101238B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-6c4eed1389624149a76331714ac9fde2
출처 메모uspto-grants-2012_01