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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 451299Erstellt: 26. Oktober 2026

Hydrochloric Acid → 4-Amino-1-N-Cbz-piperidine

https://huagongshe.com/reaction/451299

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
EduktSodium HydroxideHCID 14798—
EduktBenzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Amino-1-N-Cbz-piperidineHCID 17846640—

Reaktionsbedingungen

Temperatur32.5 °C

Reaktionsschritte

4-(N—BOC amino)-CBz piperidine (24.4 kg 73.42 mol), THF (65 kg) and 5 M HCl (23.0 kg, 110.13 mol) were combined and heated to 30-35° C. for ˜2 hours, and then at 55° C. overnight. After cooling the reaction mixture to 10° C., dichloromethane (97 kg) and 10M NaOH (7.97 kg, 145.12 mol) were added, while keeping the temperature at <25° C. The phases were separated and the organic phase was washed with 25 wt % NaCl solution (27.5 kg). The washed organic phase was distilled at atmospheric pressure to a volume of 70 L. Dichloromethane (162 kg) was then added, and the mixture was concentrated by distillation to a volume of 120 L to give the title product as a solution in DCM (17.2 kg. 100%.). 1H NMR (CDCl3) 7.33 (5H, m), 5.14 (2H, s), 4.14 (2H, br s), 2.87 (3H, m), 1.83 (2H, m), 1.66 (3H, m) and 1.28 (2H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08487093B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-bf05f1b982934de486754cfd4c208345
Quellennotizuspto-grants-2013_07