Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1171657Erstellt: 25. Oktober 2026

Ammonium Chloride → (E)-3-[(Pyrrol-2-yl)methylidene]-1-(triphenylmethyl)piperidin-4-one

https://huagongshe.com/reaction/1171657

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt1-Tritylpiperidin-4-oneHCID 2748414—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
Edukttert-Butyl 2-formyl-1H-pyrrole-1-carboxylateHCID 5057005—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(E)-3-[(Pyrrol-2-yl)methylidene]-1-(triphenylmethyl)piperidin-4-oneHCID 2313876935%

Reaktionsschritte

To a solution of 1-(triphenylmethyl)piperidin-4-one (17.00 g) in tetrahydrofuran (400 ml) was added dropwise a 0.5N solution of potassium bis(trimethylsilyl)amide in toluene (100 ml) at −70° C., and the resulting mixture was stirred at the same temperature for 20 minutes. Subsequently, to the reaction mixture was added dropwise a solution of 1-(t-butoxycarbonyl)pyrrole-2-carbaldehyde (11.00 g) in tetrahydrofuran (100 ml) at −70° C., and the resulting mixture was stirred at the same temperature for 1 hour. After saturated aqueous ammonium chloride solution was added, the resulting reaction mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution and the organic layer was dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate, hexane, and dichloromethane (1:3:1) as the eluent to afford the title compound (7.26 g, yield: 35%) as a yellow amorphous solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07829580B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-c8197e42b60344b9ba78b7da8b756cb7
Quellennotizuspto-grants-2010_11