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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1713109Erstellt: 25. Oktober 2026

tert-Butanol → HCID 46253561, Verbindung

https://huagongshe.com/reaction/1713109

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktMorpholine-4-carboximidamide HydrobromideHCID 2806564—
EduktPotassium tert-butoxideHCID 23665647—
Edukttert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylateHCID 53395404—
LösungsmittelEthanolHCID 702—
ProduktHCID 46253561HCID 46253561—

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

To a 500 ml round bottom flask charged with anhydrous EtOH (150 ml) under nitrogen at 0° C. are added morpholine-4-carboxamidine hydrobromide (10.50 g, 50 mmol), tert-butyl-3-[(dimethylamino)methylene]-4-oxo-1-piperidinecarboxylate (12.7 g, 50 mmol, 1.0 eq.), and potassium t-butoxide in t-butanol (11.0M, 100 ml, 100 mmol, 2.0 eq.). The resulting mixture is stirred at 75° C. for 16 hr. The solvent is evaporated under reduced pressure, and the residue is taken up in DCM (300 ml), washed with water and brine, dried (Na2SO4) and concentrated. The residue is purified by silica gel chromatography (Hexane/EtOAc 1:1) to give the title compound. MS (+VE) m/z 321.1 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07795262B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-7a1b2c88050e4b0d8a190e35d0435036
Quellennotizuspto-grants-2010_09