Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602342Erstellt: 26. Oktober 2026

4-Chloroaniline → tert-butyl (R)-2-(4-chlorophenylcarbamoyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/602342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChloroanilineHCID 7812—
Edukt2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
Edukt(2R)-1-[(tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 688022—
LösungsmittelTolueneHCID 1140—
Produkttert-butyl (R)-2-(4-chlorophenylcarbamoyl)pyrrolidine-1-carboxylateHCID 9138711—

Reaktionsschritte

4.82 g (19.5 mmol) of ethyl 2-ethoxy-1,2-dihydroquinoline-1-carboxylate (EEDQ) are added to a suspension of 2.80 g (13.0 mmol) of N-Boc-D-proline and 1.66 g (13.0 mmol) of 4-chloroaniline in 50 ml of toluene, and the mixture is stirred at room temperature for 3 hours. The reaction mixture is filtered, and petroleum ether is added to the filtrate. The precipitate formed is filtered off and dried, giving tert-butyl (R)-2-(4-chlorophenylcarbamoyl)pyrrolidine-1-carboxylate as colourless crystals; ESI 325.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07906516B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-3d4be8b56c6e4a41abd341a00e524224
Quellennotizuspto-grants-2011_03