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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 866056Erstellt: 25. Oktober 2026

Ethyl 4-piperidinecarboxylate → ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylate

https://huagongshe.com/reaction/866056

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-piperidinecarboxylateHCID 70770—
Edukt4-(Allyloxy)benzaldehydeHCID 95942—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produktethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylateHCID 1904093498,9%

Reaktionsschritte

The reaction conditions taught by A. E. Moormann, Syn. Comm., 23(6), 789-795 (1993) were used in the following preparation. To a stirred solution of 4.8 grams (0.030 mole) of ethyl piperidin-4-ylcarboxylate and 4.9 grams (0.030 mole) of 4-(2-propen-1-yloxy)benzaldehyde in 50 mL of ethanol was added 3.8 mL (0.030 mole) of borane-pyridine complex. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 18 hours. The reaction mixture was then taken up in water and extracted with methylene chloride. The organic layer was washed with water and dried with magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure, yielding 9.0 grams of ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylate. The NMR spectrum was consistent with the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05569664
Quelldatensatzuspto-grants-1996_10
ORD IDord-3e0acf32c1dd480bbf13d4c2f7d72993
Quellennotizuspto-grants-1996_10