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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432931Erstellt: 25. Oktober 2026

4-Fluorobenzoyl chloride → (4-Fluorophenyl)[2-methoxy-5-(2,6-dimethyl-4-nitrophenoxy)phenyl]methanone

https://huagongshe.com/reaction/432931

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluorobenzoyl chlorideHCID 67879—
Edukt4-(4-Methoxy-phenoxy)-3,5-dimethyl-nitrobenzeneHCID 10084672—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelDichloromethaneHCID 6344—
Produkt(4-Fluorophenyl)[2-methoxy-5-(2,6-dimethyl-4-nitrophenoxy)phenyl]methanoneHCID 1004620553,1%

Reaktionsschritte

To a solution of 4-(4-methoxy-phenoxy)-3,5-dimethyl-nitrobenzene (2.7 g, 10 mmol) and p-fluorobenzoyl chloride (4.0 g, 3.0 mL, 25 mmol) in methylene chloride (10 mL) was added titanium tetrachloride (1M in methylene chloride, 50 mL, 50 mmol). The reaction mixture was stirred at room temperature for 3 d, poured into ice (100 g), and stirred 1 h. The organic layer was separated and the aqueous layer was extracted with methylene chloride (3×50 mL). The combined organic extracts were washed with 5% sodium carbonate (200 mL), brine (150 mL), dried and concentrated. The residue was triturated with ether-petroleum ether. The solid was collected by filtration to give the title compound of Step A (2.1 g) as a tan solid. MS (APCl−Calc.: 395.2, Found: 394.2 (M−1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06664291B2
Quelldatensatzuspto-grants-2003_12
ORD IDord-9a1ba7343789476e8f187b3516ee3dc7
Quellennotizuspto-grants-2003_12