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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425694Generated: October 25, 2026

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

https://huagongshe.com/reaction/1425694

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 numberUS08933065B2
Source datasetuspto-grants-2015_01
ORD IDord-f498d336e90049d89ed5ea838d3a0d2f
Source noteuspto-grants-2015_01