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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73127Generated: October 25, 2026

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

https://huagongshe.com/reaction/73127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-CyanophenolHCID 13019—
Reactant3-Fluorobenzyl bromideHCID 68007—
ReactantD-AbequoseHCID 160540—
SolventAcetoneHCID 180—
Product4-[(3-Fluorophenyl)methoxy]benzonitrileHCID 222938387.2%

Reaction Steps

(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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829033B2
Source datasetuspto-grants-2014_09
ORD IDord-8541a7b1c057457fbe210b8acc3919ea
Source noteuspto-grants-2014_09