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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 482027Erstellt: 25. Oktober 2026

Dimethylformamide → 4-(Piperidin-1-yl)benzaldehyde

https://huagongshe.com/reaction/482027

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt1-PhenylpiperidineHCID 20038—
EduktPhosphorus oxychlorideHCID 24813—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt4-(Piperidin-1-yl)benzaldehydeHCID 29135440%

Reaktionsschritte

To a solution of 2.3 mL (mmoles) of N,N-dimethylformamide in 10 mL of 1,2-dichloroethane was added dropwise 2.8 mL (30 mmoles) of phosphorus oxychloride at 0°C. The ice-bath was removed and the reaction mixture was stirred for 15 min. 1-Phenylpiperidine (3.2 mL, 20 mmoles) was added to the above solution portionwise and the reaction mixture was refluxed overnight. The reaction mixture was poured into ice-cold 2N sodium hydroxide solution and stirred at room temperature for 1 h. The organic layer was separated and the aqueous layer was extracted with 2×20 mL of ethyl acetate. The combined organic layer was washed with brine until pH=7, dried over anhydrous sodium sulfate and evaporated. The residue was separated on a silica gel column eluting with ethyl acetate and hexane to afford 1.5 g (40%) of the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05792783
Quelldatensatzuspto-grants-1998_08
ORD IDord-8a260c01b63a431c989f5a0123438dcb
Quellennotizuspto-grants-1998_08