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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44412Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/44412

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
PatentnummerUS08541426B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-4bb213a94a2b4446855d46d65502409d
Quellennotizuspto-grants-2013_09