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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1382707Erstellt: 26. Oktober 2026

N-(1-benzylpiperidin-4-yl)-2,2,2-trifluoroacetamide → 2,2,2-trifluoro-N-(piperidin-4-yl)acetamide

https://huagongshe.com/reaction/1382707

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(1-benzylpiperidin-4-yl)-2,2,2-trifluoroacetamideHCID 1531300—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt2,2,2-trifluoro-N-(piperidin-4-yl)acetamideHCID 10774253—

Reaktionsschritte

A suspension of 92 g of 1-benzyl 4-trifluoromethylcarbonylamino piperidine (X) and 9 g of wet 10% palladium on charcoal in 1000 ml of methanol is left under agitation for 8 days in a hydrogen atmosphere at room temperature. Then it is filtered, the filtrate is evaporated and the residue chromatographed on a silica column (M.P.L.C.). By eluting with pure methanol, 44 g of the expected product are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04808582
Quelldatensatzuspto-grants-1989_02
ORD IDord-86bc40a3c3864ef5aaf2999be51a3d40
Quellennotizuspto-grants-1989_02