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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1869645Erstellt: 25. Oktober 2026

Pyridine → (2S)-1-(2-bromoacetyl)pyrrolidine-2-carbonitrile

https://huagongshe.com/reaction/1869645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktBromoacetyl bromideHCID 61147—
Edukt(2S)-pyrrolidine-2-carbonitrileHCID 5706552—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S)-1-(2-bromoacetyl)pyrrolidine-2-carbonitrileHCID 1103127682,6%

Reaktionsschritte

To a cold solution (−10° C.) of bromoacetyl bromide (2.0 g, 10.0 mmol) in CH2Cl2 (30 mL), a solution of (S)-pyrrolidine-2-carbonitrile (480 mg, 5.0 mmol) and pyridine (1.4 g, 210 mmol) together with a catalytic amount of DMAP (50 mg) in CH2Cl2 (10 mL) was added over a 30 minute period. After stirring for about 10 minutes, the reaction temperature was gradually increased to room temperature. Stirring at room temperature was continued overnight. The residue was diluted with CH2Cl2 (60 mL), washed with ice water and cold 10% sodium bicarbonate aqueous solution to give crude product (1.01 g; yield of 93%). Column chromatography purification of the crude product resulted in pure 1-(2-bromo-acetyl)-(S)-pyrrolidine-2-carbonitrile (892 mg; 82.6% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07638638B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-215d032144eb482e9e54cb7de404639e
Quellennotizuspto-grants-2009_12