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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1791858생성일: 2026년 10월 27일

Benzenesulfonyl chloride → N-{5-[2-(4-Cyanophenyl)ethoxy]-2-methylphenyl}benzenesulfonamide

https://huagongshe.com/reaction/1791858

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Sodium BicarbonateHCID 516892—
반응물Amino-5-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 22033532—
용매PyridineHCID 1049—
생성물N-{5-[2-(4-Cyanophenyl)ethoxy]-2-methylphenyl}benzenesulfonamideHCID 22033468100%

반응 단계

Benzenesulfonyl chloride (22 μL; 0.17 mmol) was added to a cold solution (ice:water temperature) of amino-5-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene (0.041 g; 0.16 mmol; from step (ii) above) in pyridine (4 mL) The reaction flask was left overnight in a refrigerator. NaHCO3/aq (sat.) was added and the solution extracted twice with EtOAc. The combined organic phases were washed with water, HCl/aq (2M) and water. Drying (MgSO4) and evaporation of the solvent in vacuo afforded 0.062 g (100%) of the sub-title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07074820B2
출처 데이터셋uspto-grants-2006_07
ORD IDord-b6cc1b52f1bd4a2782218856645c0bae
출처 메모uspto-grants-2006_07