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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768134Generated: October 27, 2026

p-Fluoronitrobenzene → 1-(3-Fluorobenzyloxy)-4-nitro-benzene

https://huagongshe.com/reaction/1768134

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Fluorobenzylic alcoholHCID 68008—
SolventWaterHCID 962—
Product1-(3-Fluorobenzyloxy)-4-nitro-benzeneHCID 2213791561.4%

Reaction Steps

A mixture of 5.04 g (40 mmol) 3-fluorobenzyl alcohol and 1.29 g (4 mmol) tris-(dioxa-3,6-heptyl)amine is treated with 2.47 g (44 mmol) of potassium hydroxide. The mixture is stirred at RT for 10 min, then 5.55 g (44 mmol) of 4-fluoro-nitrobenzene is slowly added through a dropping funnel. The mixture is kept for 45 min at 80° C., cooled to RT and diluted with about 75 ml water. Extraction with ethyl acetate and washing with 2M aqueous hydrochloric acid yields a yellowish organic phase, which is dried and evaporated. The residue is recrystallised from methanol to give 6.07 g (61%) of the title compound. Yellow crystals, mp=104–105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235581B2
Source datasetuspto-grants-2007_06
ORD IDord-52ae011dae614c82add029e1fb88c0cf
Source noteuspto-grants-2007_06