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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2251314Erstellt: 27. Oktober 2026

Benzene, 1-bromo-3-nitro- → 1-(3-Nitrophenyl)pyrrolidine

https://huagongshe.com/reaction/2251314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 1-bromo-3-nitro-HCID 11457—
EduktPyrrolidineHCID 31268—
EduktSodium t-butoxideHCID 23676156—
LösungsmittelTolueneHCID 1140—
Produkt1-(3-Nitrophenyl)pyrrolidineHCID 69826779%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 3-bromonitrobenzene (2.02 g, 10 mmol) in toluene (33 mL) and pyrrolidine (1.0 mL, 12 mmol) was added sodium t-butoxide (1.92 g, 20 mmol) and the solution was deoxygenated by passing a nitrogen through the solution at room temperature for 15 minutes. BINAP and tris(dibenzylideneacetone)dipalladium(0) complex were subsequently added as a solid and the nitrogen bubbling was continued for an additional 5 minutes. The mixture was heated at 100° C. overnight. The reaction mixture was then cooled and partitioned between water and ethyl acetate. The organic layer was washed once with brine solution and dried over anhydrous sodium sulfate. The ethyl acetate was decanted and evaporated under reduced pressure to give the desired 1-(3-nitrophenyl)pyrrolidine as a red oil (1.5 g, 79%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07319111B2
Quelldatensatzuspto-grants-2008_01
ORD IDord-f79c588c6b9b490eb59632ae718f193e
Quellennotizuspto-grants-2008_01