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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 469289Erstellt: 24. Oktober 2026

Acetic Acid → (1-Benzylpiperidin-4-yl)-[2-(5-methoxy-2-nitrophenyl)-ethyl]-amine

https://huagongshe.com/de/reaction/469289

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPotassium CarbonateHCID 11430—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-Benzyl-2-piperidoneHCID 5170076—
Edukt2-(5-Methoxy-2-nitrophenyl)ethan-1-amineHCID 18621975—
LösungsmittelDichloromethaneHCID 6344—
Produkt(1-Benzylpiperidin-4-yl)-[2-(5-methoxy-2-nitrophenyl)-ethyl]-amineHCID 21109931100%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Under a nitrogen atmosphere a mixture of 9.98 g (50.9 mmol) 2-(5-methoxy-2-nitrophenyl)-ethylamine, 9.80 mL (54.9 mmol) N-benzylpiperidone and 6.30 mL (114 mmol) acetic acid in 270 mL DCM was cooled to 0° C. in an ice bath. At this temperature 14.2 g (67.0 mmol) sodium triacetoxyborohydride were added batchwise within 20 min. The reaction mixture was stirred for a further 4 h at 0° C. and left to warm up to RT overnight. Then the mixture was combined with 400 mL of a 15% (w/v) aqueous potassium carbonate solution and stirred for 1 h at RT. The organic phase was separated off, dried and concentrated by rotary evaporation. 18.8 g of the desired product were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629137B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-3e1c2f221c9e4506885fd66d5bd83c5b
Quellennotizuspto-grants-2014_01