Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 352434Erstellt: 24. Oktober 2026

Hydrochloric Acid → HCID 22712048, Verbindung

https://huagongshe.com/de/reaction/352434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktCyclopropanecarboxaldehydeHCID 123114—
Edukt1-benzyl-N-methylpiperidin-4-amineHCID 4136128—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
ProduktHCID 22712048HCID 2271204895%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

18.9 g of 1-benzyl-4-methylaminopiperidine in the form of the oil prepared in a) are taken up in 250 ml of methanol, combined with 8.3 g of cyclopropane carboxaldehyde and 11.3 g of sodium cyanoborohydride. The mixture is stirred for 5 hours at 40-50° C., then for about 16 hours at ambient temperature. It is then acidified with 2 N hydrochloric acid, evaporated to dryness in vacuo and the residue is taken up in water. It is washed with ether, made alkaline with concentrated sodium hydroxide solution and extracted with ether/ethyl acetate. The organic extract is dried over sodium sulphate and freed from solvents in vacuo. 22.7 g of 1-benzyl-4-(cyclopropylmethyl-methyl-amino)-piperidine are obtained as a yellowish oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06747044B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-f8daccd7025a4cf39fdc5c8693be6b22
Quellennotizuspto-grants-2004_06