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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 546615Erstellt: 26. Oktober 2026

(4-Nitrophenyl)(pyrrolidin-1-yl)methanone → 4-(Pyrrolidin-1-ylcarbonyl)aniline

https://huagongshe.com/reaction/546615

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(4-Nitrophenyl)(pyrrolidin-1-yl)methanoneHCID 386112—
EduktAmmonium formateHCID 2723923—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt4-(Pyrrolidin-1-ylcarbonyl)anilineHCID 577800115,8%

Reaktionsschritte

To a solution of 1.28 g of 1-(4-nitrobenzoyl)pyrrolidine obtained in stage a) below in 50 mL of methanol are added, under argon, 4.26 g of ammonium formate and 9 mg of 10% palladium-on-charcoal. The reaction mixture is stirred at room temperature for 5 hours and then filtered through Celite and concentrated under reduced pressure. The residue is taken up in water and extracted with ethyl acetate. The organic phase is then washed with saturated sodium chloride solution, dried over magnesium sulphate, filtered and concentrated under reduced pressure to give 1.28 g of 4-(pyrrolidin-1-ylcarbonyl)aniline, the characteristics of which are as follows:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07935819B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-976bb117e69147dfb22da00f6c7266ef
Quellennotizuspto-grants-2011_05