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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73127생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-CyanophenolHCID 13019—
반응물3-Fluorobenzyl bromideHCID 68007—
반응물D-AbequoseHCID 160540—
용매AcetoneHCID 180—
생성물4-[(3-Fluorophenyl)methoxy]benzonitrileHCID 222938387.2%

반응 단계

(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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829033B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8541a7b1c057457fbe210b8acc3919ea
출처 메모uspto-grants-2014_09