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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1723826생성일: 2026년 10월 27일

Triethylamine → 1-(Methylsulfonyl)-4-[4-(2,2,2-trifluoroethoxy)phenyl]piperazine

https://huagongshe.com/reaction/1723826

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물1-[4-(2,2,2-Trifluoroethoxy)phenyl]piperazineHCID 43510344—
용매DichloromethaneHCID 6344—
생성물1-(Methylsulfonyl)-4-[4-(2,2,2-trifluoroethoxy)phenyl]piperazineHCID 2106862419.5%

반응 조건

온도0 °C

반응 단계

1-[4-(2,2,2-trifluoroethoxy)phenyl]piperazine (13.48 g, 50 mmol) was dissolved in DCM (500 mL) and cooled to 0° C. Triethylamine (29 mL, 0.2 mol) was added, followed by the dropwise addition of methanesulfonyl chloride (4.2 mL, 55 mmol). The reaction was then allowed to warm to room temperature and stir overnight, before being quenched by the addition of water. The layers were separated, and the organic phase dried (MgSO4), filtered and concentrated. The residue was recrystallised from hot ethanol to give pure 1-(methylsulfonyl)-4-[4-(2,2,2-trifluoroethoxy)phenyl]piperazine (3.3 g, 18%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07485644B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-0c7223e91e814e678a6c46b4b906b5a2
출처 메모uspto-grants-2009_02