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HRID 73127Erstellt: 23. Oktober 2026

Potassium Carbonate → 4-[(3-Fluorophenyl)methoxy]benzonitrile

https://huagongshe.com/de/reaction/73127

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-CyanophenolHCID 13019—
Edukt3-Fluorobenzyl bromideHCID 68007—
EduktD-AbequoseHCID 160540—
LösungsmittelAcetoneHCID 180—
Produkt4-[(3-Fluorophenyl)methoxy]benzonitrileHCID 222938387,2%

Reaktionsschritte

(Nakamoto, Kazutaka; Tsukada, Itaru; Tanaka, Keigo; Matsukura, Masayuki; Haneda, Toru; Inoue, Satoshi; Ueda, Norihiro; Abe, Shinya; Hata, Katsura; Watanabe, Naoaki, WO 2005033079 (2005)). A mixture of 4-cyanophenol (11.91 g, 100.0 mmol), K2CO3 (55.20 g, 400.0 mmol), and 3-fluorobenzylbromide (22.68 g, 120.0 mmol) were heated in acetone (400 mL) at reflux (5 h). The volatiles were evaporated and the residue was diluted in CH2Cl2 (300 mL), and then washed with H2O (500 mL), dried (MgSO4), and concentrated in vacuo to give white needles (19.81 g, 87%): Rf=0.45 (hexanes/EtOAc 9/1); mp 104-105° C.; 1H NMR (CDCl3) δ 5.11 (s, CH2O), 6.98-7.20 (m, 5 ArH), 7.33-7.41 (m, 1 ArH), 7.59 (d, J=8.7 Hz, 2 ArH); HRMS (M+Na+) (ESI+) 250.0641 [M+Na+] (calcd for C14H10NONa+250.0641).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829033B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8541a7b1c057457fbe210b8acc3919ea
Quellennotizuspto-grants-2014_09