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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103119Generated: November 1, 2026

3-Fluoroanisole → HCID 22475212, compound

https://huagongshe.com/reaction/2103119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluoroanisoleHCID 9975—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventNitrobenzeneHCID 7416—
ProductHCID 22475212HCID 2247521225%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a cold (5° C.) mixture of aluminium trichloride (144 g, 1.08 mol, 1.13 eq.) in nitrobenzene (450 mL) was slowly added a solution of 4-fluorobenzoyl chloride (120 mL, 1 mol, 1.05 eq.) in nitrobenzene (200 mL). 3-fluoroanisole (108.5 mL, 0.95 mol) was slowly added to the reaction mixture. The cooling bath was removed and the reaction mixture was stirred 3 h at 20° C., and poured into ice-water. The aqueous layer was extracted with dichloromethane (2 times). The combined organic layers were dried over sodium sulfate, filtered and the volatiles were removed in vacuo. The crude mixture was crystallized in cyclohexane, filtered and the solid was washed with cyclohexane. The solid was dried in vacuo, affording the title compound (57.78 g, 25%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576088B2
Source datasetuspto-grants-2009_08
ORD IDord-cc0452c032674dd5a4c502ee0f47248a
Source noteuspto-grants-2009_08