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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561451Erstellt: 27. Oktober 2026

1-Bromo-2-chloro-4-fluorobenzene → 2-(2-Chloro-4-fluorobenzoyl)cyclopropanecarbonitrile

https://huagongshe.com/reaction/561451

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-2-chloro-4-fluorobenzeneHCID 2733406—
EduktMagnesiumHCID 5462224—
Edukt2-Cyano-N-methoxy-N-methylcyclopropanecarboxamideHCID 58392506—
Katalysator1,1-DibromoethaneHCID 11201—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(2-Chloro-4-fluorobenzoyl)cyclopropanecarbonitrileHCID 58392501—

Reaktionsschritte

A solution of 24.0 g (115 mmol) of 2-chloro-4-fluorobromobenzene in 20 ml of diethyl ether was added dropwise to 2.92 g (120 mmol) of magnesium turnings in 780 ml of diethyl ether, activated by adding a few drops of dibromoethane, and the reaction mixture was heated under reflux overnight. The reaction solution was added dropwise under argon to a solution of 17.7 g (68.8 mmol) of the compound from Example 73A in 300 ml of THF, and the reaction mixture was stirred initially at RT overnight and then under reflux for 8 h. It was concentrated and taken up in ethyl acetate and saturated aqueous ammonium chloride solution, the phases were separated, and the organic phase was washed with water and saturated aqueous sodium bicarbonate solution, dried over magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate gradient) to result in 2.20 g (14% of theory) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063234B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-a3fb5359405a4c2cabdc84b5251e820d
Quellennotizuspto-grants-2011_11