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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2212180Erstellt: 26. Oktober 2026

Acetic Acid → Methyl 3-aminopiperidine-1-carboxylate

https://huagongshe.com/reaction/2212180

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
Edukt3-(Trityl-amino)-piperidine-1-carboxylic acid methyl esterHCID 69652409—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 3-aminopiperidine-1-carboxylateHCID 2227309895,6%

Reaktionsschritte

Add acetic acid saturated with HCl(g) (100 mL, ˜3N in HCl) to 3-(trityl-amino)-piperidine-1-carboxylic acid methyl ester (6.51 g, 16.2 mmol). Stir the solution vigorously at room temperature for 2 hours. Concentrate the reaction, follow this by addition of acetonitrile and concentration to assist in the removal of acetic acid (×2). Partition the resulting material between 1N HCl and ethyl acetate, separate the layers, extract the organic layer with 1N HCl. Basify the combined aqueous layers with 5N sodium hydroxide, extract with 20% isopropanol/chloroform (×3). Dry the combined organic layers over magnesium sulfate and concentrate to give 2.45 g of the title compound as a white solid, 95% yield. 1H NMR: consistent with structure. MS (ion spray) 158 (M+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07101891B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-8d411f7d4713493f87e38178998d2b8d
Quellennotizuspto-grants-2006_09