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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407834Erstellt: 25. Oktober 2026

N-bromobutanimide → 2-Bromo-3-methoxycyclopent-2-enone

https://huagongshe.com/reaction/407834

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt3-Methoxycyclopent-2-en-1-oneHCID 643476—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt2-Bromo-3-methoxycyclopent-2-enoneHCID 11095426—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

N-Bromosuccinimide (24.92 g, 0.140 mol) is added, portionwise, over 1 hour to a stirred solution of 3-methoxycyclopent-2-enone (14.95 g, 0.133 mol) in 1,2-dichloroethane (300 ml) at 0° C. in an amber flask. The reaction mixture is stirred at 0° C. for a further 90 minutes and then any remaining solid is removed by filtration. The filtrate is evaporated to dryness under reduced pressure, the resultant solid is dissolved in warm toluene (600 ml) and washed quickly with ice-cold water (2×100 ml). The organic phase is dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated under reduced pressure until approximately 150 ml remains. The residue is cooled with an ice bath and left for 30 minutes. The resultant solid is removed by filtration, washed with hexane (50 ml) and air-dried to give 2-bromo-3-methoxycyclopent-2-enone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754242B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-40358d0d904d4f59826a9b3259dccb2d
Quellennotizuspto-grants-2014_06