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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | 3-Fluorobenzyl bromide | HCID 68007 | — |
| Reactant | D-Abequose | HCID 160540 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-[(3-Fluorophenyl)methoxy]benzonitrile | HCID 2229383 | 87.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829033B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8541a7b1c057457fbe210b8acc3919ea |
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| Source note | uspto-grants-2014_09 |
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