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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2916생성일: 2026년 10월 24일

p-Toluenesulfonic acid → Triphenylsulfonium p-toluenesulfonate

https://huagongshe.com/ko/reaction/2916

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Triphenylsulfonium BromideHCID 11984010—
용매WaterHCID 962—
생성물Triphenylsulfonium p-toluenesulfonateHCID 2187246773.1%

반응 단계

A solution of triphenylsulfonium bromide (6.87 g, 20.0 mmol) and p-toluenesulfonic acid (3.80 g, 20.0 mmol) in water (100 ml) was heated at a gentle reflux for 15 hours under nitrogen. After cooling to room temperature, the clear solution was extracted with dichloromethane (4×75 ml). The combined organic extracts were washed with water until neutral (4×75 ml) and dried (MgSO4 ). The solvent was removed under reduced pressure and the residue dried by heating at 80° C. in vacuo for 36 hours to give a crude onium salt as a off-white solid (6.35 g). Recrystallization from acetone-ethyl acetate gave triphenylsulfonium rosylate as a white crystalline solid (5.72 g, 66%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731364
출처 데이터셋uspto-grants-1998_03
ORD IDord-859a3ba4fca04957adca8f06dc6bef2a
출처 메모uspto-grants-1998_03