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HRID 276771Erstellt: 24. Oktober 2026

2-Bromo-1-(3,4-dichlorophenyl)ethanone → HCID 178477975, Verbindung

https://huagongshe.com/de/reaction/276771

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-1-(3,4-dichlorophenyl)ethanoneHCID 244751—
EduktSodium BicarbonateHCID 516892—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt6-Chloro-3-pyridinecarbonitrileHCID 5152094—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178477975HCID 178477975—

Reaktionsschritte

Lithium hexamethyldisilazide (41.5 mL of a 1.0 M solution in THF) was added to a solution of 2-chloro-5-cyanopyridine (5.24 g) in THF (10 mL). The resultant mixture was stirred at room temperature for 30 min, and then 13 mL saturated aqueous sodium bicarbonate and 5 mL water were added to the reaction mixture. A solution of 3,4-dichlorophenacyl bromide (10.13 g) in chloroform (150 mL) was added in two portions approximately 15 min apart. The resultant mixture was stirred for 72 hours, and the reaction mixture was filtered. The filter cake was triturated with dichloromethane (50 mL) to provide 2-Chloro-5-[4-(3,4-dichloro-phenyl)-1H-imidazol-2-yl]-pyridine (10.46 g). MS m/z 324 (M+), 326 (M++2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06355635B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-ee9b6e165ef34b6fb9cf15324b2925e1
Quellennotizuspto-grants-2002_03