Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41968Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2,6-DifluorobenzaldehydeHCID 136284—
Edukt4-Methanesulfonylpiperidine hydrochlorideHCID 23061698—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-Fluoro-6-(4-methanesulfonylpiperidine-1-yl)benzaldehydeHCID 5813796284%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536172B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-7604022984de470db2eaaeb7e6b15206
Quellennotizuspto-grants-2013_09