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HRID 1490148생성일: 2026년 10월 25일

N-Ethyl-p-toluenesulfonamide → N-Ethyl-N-(3-chloropropyl)-p-toluenesulfonamide

https://huagongshe.com/reaction/1490148

반응식

참여 물질

역할이름HCID투입량
반응물N-Ethyl-p-toluenesulfonamideHCID 6637—
반응물1,3-DichloropropaneHCID 8881—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물N-Ethyl-N-(3-chloropropyl)-p-toluenesulfonamideHCID 1405676242%

반응 조건

온도53 °C

반응 단계

To N-ethyl-p-toluenesulfonamide (5.01 g, 0.0251 mol) in DMF (50 mL) in a dry flask is added sodium hydride (80% in oil, 0.93 g, 0.031 mol). After gas evolution subsides, 1,3-dichloropropane (22.48 g, 0.199 mol) is added. The mixture is heated at 53° C. for 10 h then cooled and poured into ice water (300 mL), which is extracted twice with ether. The combined extracts are washed with 1% sodium bisulfite, water (3×), and brine. Removal of solvent by rotary evaporation then Kugelrohr distillation gives crude product, which is chromatographed on silica gel (30% hexane/CHCl3) to furnish 2.91 g product (42%) NMR (CDCl3) δ1.15 (t, 3H), 1.9-2.2 (m, 2H), 2.44 (s, 3H), 3.11-3.35 (m, 4H), 3.6 (t, 2H), 7.3 (d, 2H), 7.74 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05681837
출처 데이터셋uspto-grants-1997_10
ORD IDord-23c25065507e40958c562610e7847640
출처 메모uspto-grants-1997_10