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HRID 1425694Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1425694

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
PatentnummerUS08933065B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-f498d336e90049d89ed5ea838d3a0d2f
Quellennotizuspto-grants-2015_01