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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2,6-Difluorobenzaldehyde | HCID 136284 | — |
| Edukt | 4-Methanesulfonylpiperidine hydrochloride | HCID 23061698 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 2-Fluoro-6-(4-methanesulfonylpiperidine-1-yl)benzaldehyde | HCID 58137962 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536172B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-7604022984de470db2eaaeb7e6b15206 |
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| Quellennotiz | uspto-grants-2013_09 |
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