Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1169014Erstellt: 26. Oktober 2026

Acetic Acid → 1-benzyl-N,4-dimethylpiperidin-3-amine

https://huagongshe.com/reaction/1169014

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktMethanolHCID 887—
EduktMethylamineHCID 6329—
Edukt1-Benzyl-4-methylpiperidin-3-oneHCID 12084828—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-benzyl-N,4-dimethylpiperidin-3-amineHCID 994388969%

Reaktionsschritte

To a stirred solution of 1-benzyl-4-methyl-piperidin-3-one (2.3 grams, 11.5 mmol), prepared by the methods of Iorio, M. A. and Damia, G., Tetrahedron, 26, 5519 (1970) and Grieco et al., Journal of the American Chemical Society, 107, 1768 (1985), (modified using 5% methanol as a co-solvent), both references are incorporated by reference in their entirety, dissolved in 23 mL of 2 M methylamine in tetrahydrofuran was added 1.4 mL (23 mmol) of acetic acid and the resulting mixture stirred in a sealed tube for 16 hours at room temperature. Triacetoxy sodium borohydride (4.9 grams, 23 mmol) was added and the new mixture stirred at room temperature in a sealed tube for 24 h, at which time, the reaction was quenched upon addition of 1 N sodium hydroxide (50 mL). The reaction mixture was then extracted 3×80 mL with ether, the combined ether layers dried over sodium sulfate (Na2SO4) and concentrated to dryness in vacuo affording 1.7 grams (69%) of the title compound as a white solid. LRMS: 219.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06627754B2
Quelldatensatzuspto-grants-2003_09
ORD IDord-27b13ea3b72545d8898f9bbc83291099
Quellennotizuspto-grants-2003_09