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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41968생성일: 2026년 10월 23일

Diisopropylethylamine → 2-Fluoro-6-(4-methanesulfonylpiperidine-1-yl)benzaldehyde

https://huagongshe.com/ko/reaction/41968

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2,6-DifluorobenzaldehydeHCID 136284—
반응물4-Methanesulfonylpiperidine hydrochlorideHCID 23061698—
용매AcetonitrileHCID 6342—
생성물2-Fluoro-6-(4-methanesulfonylpiperidine-1-yl)benzaldehydeHCID 5813796284%

반응 조건

온도80 °C

반응 단계

In a 250 mL round bottom flask, 2,6-difluorobenzaldehyde (7.12 g, 5.4 mL, 50.1 mmol), 4-methanesulfonylpiperidine hydrochloride (10 g, 50.1 mmol) and DIPEA (7.77 g, 60.1 mmol) were combined with acetonitrile (75 mL). The mixture was stirred and heated at 80° C. overnight. The mixture was evaporated and extracted with dichloromethane and citric acid solution. The organic layer was washed with brine, dried over sodium sulfate, and evaporated. The crude solid was triturated with cold ethyl acetate to afford 2-fluoro-6-(4-methanesulfonylpiperidine-1-yl)benzaldehyde (12 g, 84% yield). LC-MS calcd for C13H16FNO3S (m/e) 285.08, obsd 286.0 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536172B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-7604022984de470db2eaaeb7e6b15206
출처 메모uspto-grants-2013_09